Method of making an array of nucleic acid colonies

ABSTRACT

A method of making an array of nucleic acid colonies, including the steps of (a) providing a substrate having a patterned surface of features, wherein the features are spatially organized in a repeating pattern on the surface of the substrate; (b) contacting the substrate with a solution of different target nucleic acids to seed no more than a subset of the features that contact the solution; (c) amplifying the nucleic acids on the subset of features; and (d) repeating steps (b) and (c) to increase the number of features that are seeded with a nucleic acid, thereby making an array of nucleic acid colonies.

REFERENCE TO RELATED APPLICATIONS

This is a continuation of non-provisional application U.S. Ser. No.12/641,104, filed on Dec. 17, 2009, which claims priority to U.S.Provisional Application No. 61/140,566, filed on Dec. 23, 2008, each ofwhich is incorporated herein by reference in its entirety.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH

This invention was made with Government support under NIH GrantR501HG003571-06 awarded by the PHS. The Government has certain rights inthe invention.

REFERENCE TO SEQUENCE LISTING

The present application incorporates by reference the entirety of theSequence Listing that was filed in computer readable form on Dec. 17,2009, in connection with U.S. Ser. No. 12/641,104 filed on Dec. 17,2009.

FIELD OF THE INVENTION

The present technology relates to molecular sciences, such as genomics.More particularly, the present technology relates to nucleic acidsequencing.

BACKGROUND

The detection of specific nucleic acid sequences present in a biologicalsample has been used, for example, as a method for identifying andclassifying microorganisms, diagnosing infectious diseases, detectingand characterizing genetic abnormalities, identifying genetic changesassociated with cancer, studying genetic susceptibility to disease, andmeasuring response to various types of treatment. A common technique fordetecting specific nucleic acid sequences in a biological sample isnucleic acid sequencing.

Nucleic acid sequencing methodology has evolved significantly from thechemical degradation methods used by Maxam and Gilbert and the strandelongation methods used by Sanger. Today several sequencingmethodologies are in use which allow for the parallel processing ofthousands of nucleic acids all in a single sequencing run. As such, theinformation generated from a single sequencing run can be enormous.

SUMMARY

The present technology relates to methods for obtaining nucleic acidsequence information. Such methods can permit long read lengths oftarget nucleic acids.

Some methods described herein include the steps of (a) providing a firstsequencing reagent to a target nucleic acid in the presence of apolymerase, wherein the first sequencing reagent includes at least twodifferent nucleotide monomers, and (b) providing a second sequencingreagent to the target nucleic acid, wherein the second sequencingreagent comprises one or more nucleotide monomers, at least one of theone or more nucleotide monomers being different from the nucleotidemonomers present in the first sequencing reagent, and wherein the secondsequencing reagent is provided subsequent to providing the firstsequencing reagent, whereby sequence information for at least a portionof the target nucleic acid is obtained.

In some embodiments of the methods described herein, the at least twodifferent nucleotide monomers of the first sequencing reagent areseparately provided to the target nucleic acid.

In some embodiments of the methods described herein, the at least twodifferent nucleotide monomers of the first sequencing reagent can beprovided together to the target nucleic acid.

Other embodiments of the above-described methods, can further includerepeating the method steps.

In some embodiments of the above-described methods, the polymeraseextends a polynucleotide strand. Such embodiments can further includedetecting the incorporation of at least one nucleotide monomer into thepolynucleotide strand. In certain embodiments, the detecting can includedetecting pyrophosphate. In particular embodiments, the detecting caninclude detecting a label.

In some embodiments of the above-described methods, the first sequencingreagent can include no more than two nucleotide monomers. In certainembodiments, the second sequencing reagent can include two differentnucleotide monomers which are different from the two nucleotide monomersof the first sequencing reagent.

In some embodiments of the above-described methods, the first sequencingreagent can include no more than three nucleotide monomers. In certainembodiments, the second sequencing reagent can include one nucleotidemonomer which is different from the nucleotide monomers of the firstsequencing reagent.

In other embodiments of the methods described herein, the firstsequencing reagent can include a nucleotide monomer comprising a label.In still other embodiments, the second sequencing reagent can include anucleotide monomer comprising a label. In embodiments where labels areutilized, the label can be selected from the group consisting offluorescent moieties, chromophores, antigens, dyes, phosphorescentgroups, radioactive materials, chemiluminescent moieties, scattering orfluorescent nanoparticles, Raman signal generating moieties, andelectrochemical detection moieties. Further embodiments can includecleaving the label from the nucleotide monomer.

In certain embodiments of the above-described methods, the first and/orsecond sequencing reagent can include a nucleotide monomer comprising areversibly terminating moiety. In some of these embodiments, theterminating moiety can include a reversible terminating moiety.

In embodiments where nucleotide monomers include a reversibleterminator, the method of obtaining sequence information can furtherinclude cleaving the reversible terminating moiety.

In some embodiments of the methods described herein, the firstsequencing reagent and/or the second sequencing reagent includenucleotide monomers selected from the group consisting ofdeoxyribonucleotides, modified deoxyribonucleotides, ribonucleotides,modified ribonucleotides, peptide nucleotides, modified peptidenucleotides, modified phosphate sugar backbone nucleotides and mixturesthereof.

In some embodiments of the above-identified methods, the firstsequencing reagent is provided to a single target nucleic acid. In otherembodiments, the first sequencing reagent is provided simultaneously toa plurality of target nucleic acids. In such embodiments, the pluralityof target nucleic acids can include target nucleic acids havingdifferent nucleotide sequences.

In certain embodiments of the methods described herein, the firstsequencing reagent is provided to a plurality of target nucleic acids ona surface of an array in parallel. In such embodiments, the plurality oftarget nucleic acids can include target nucleic acids having the same ordifferent nucleotide sequences.

In other embodiments, the polymerase utilized in the methods describedherein includes a polymerase selected from the group consisting of a DNApolymerase, an RNA polymerase, a reverse transcriptase, and mixturesthereof. In still other embodiments, the polymerase can be athermostable polymerase or a thermodegradable polymerase.

Additional methods for obtaining nucleic acid sequence informationinclude the steps of (a) providing a first sequencing reagent to atarget nucleic acid, wherein the first sequencing reagent comprises atleast two different nucleotide monomers, (b) detecting the incorporationof a nucleotide monomer present in the first sequencing reagent into apolynucleotide strand complementary to at least a portion of the targetnucleic acid, (c) providing a second sequencing reagent to said targetnucleic acid, wherein the second sequencing reagent comprises one ormore nucleotide monomers, at least one of the one or more nucleotidemonomers being different from the nucleotide monomers present in thefirst sequencing reagent, and wherein the second sequencing reagent isprovided subsequent to providing the first sequencing reagent, and (d)detecting the incorporation of a nucleotide monomer present in thesecond sequencing reagent into the polynucleotide strand, therebyobtaining sequence information for at least a portion of the targetnucleic acid.

Other embodiments of the above-described methods, can further includerepeating the method steps.

In some embodiments of the above-described methods, the at least twodifferent nucleotide monomers of the first sequencing reagent areseparately provided to the target nucleic acid.

In some embodiments of the above-described methods, the at least twodifferent nucleotide monomers of the first sequencing reagent areprovided together to the target nucleic acid.

In certain embodiments of the above-described methods, the detecting caninclude detecting pyrophosphate. In particular embodiments, thedetecting can include detecting a label.

In some embodiments of the above-described methods, the first sequencingreagent can include no more than two nucleotide monomers. In certainembodiments, the second sequencing reagent can include two differentnucleotide monomers, which are different from the two nucleotidemonomers of the first sequencing reagent.

In some embodiments of the above-described methods, the first sequencingreagent includes no more than three nucleotide monomers. In certainembodiments, the second sequencing reagent can include one nucleotidemonomer, which is different from the nucleotide monomers of the firstsequencing reagent.

In other embodiments of the above-described methods, the firstsequencing reagent can include a nucleotide monomer comprising a label.In still other embodiments, the second sequencing reagent can include anucleotide monomer comprising a label. In embodiments where labels areutilized, the said label can be selected from the group consisting offluorescent moieties, chromophores, antigens, dyes, phosphorescentgroups, radioactive materials, chemiluminescent moieties, scattering orfluorescent nanoparticles, Raman signal generating moieties, andelectrochemical detection moieties. Further embodiments can includecleaving the label from the nucleotide monomer.

In certain embodiments of the above-described methods, the first and/orsecond sequencing reagent can include a nucleotide monomer comprising areversibly terminating moiety. In some of these embodiments, theterminating moiety can include a reversible terminating moiety.

In embodiments where nucleotide monomers include a reversibleterminator, the method of obtaining sequence information can furtherinclude cleaving the reversible terminating moiety.

In some embodiments of the above-described methods, the first sequencingreagent and/or the second sequencing reagent can include nucleotidemonomers selected from the group consisting of deoxyribonucleotides,modified deoxyribonucleotides, ribonucleotides, modifiedribonucleotides, peptide nucleotides, modified peptide nucleotides,modified phosphate sugar backbone nucleotides and mixtures thereof.

In some embodiments of the above-identified methods, the firstsequencing reagent is provided to a single target nucleic acid. In otherembodiments, the first sequencing reagent is provided simultaneously toa plurality of target nucleic acids. In such embodiments, the pluralityof target nucleic acids can include target nucleic acids havingdifferent nucleotide sequences.

In certain embodiments of the methods described herein, the firstsequencing reagent is provided to a plurality of target nucleic acids ona surface of an array in parallel. In such embodiments, the plurality oftarget nucleic acids can include target nucleic acids having the same ordifferent nucleotide sequences.

Additional methods for obtaining nucleic acid sequence information caninclude the steps of (a) providing a first sequencing reagent to atarget nucleic acid in the presence of a polymerase, wherein the firstsequencing reagent comprises at least two different nucleotide monomers,(b) removing at least a portion of the first sequencing reagent, and (c)providing a second sequencing reagent to the target nucleic acid,wherein the second sequencing reagent comprises one or more nucleotidemonomers, at least one of the one or more nucleotide monomers beingdifferent from the nucleotide monomers present in the first sequencingreagent, whereby sequence information for at least a portion of thetarget nucleic acid is obtained.

In some embodiments of the above-described methods, the at least twodifferent nucleotide monomers of the first sequencing reagent can beseparately provided to the target nucleic acid.

In some embodiments of the methods described herein, the at least twodifferent nucleotide monomers of the first sequencing reagent can beprovided together to the target nucleic acid.

Other embodiments of the above-described methods, can further includerepeating the method steps.

In some embodiments of the above-described methods, the polymeraseextends a polynucleotide strand. Such embodiments can further includedetecting the incorporation of at least one nucleotide monomer into thepolynucleotide strand. In certain embodiments, the detecting can includedetecting pyrophosphate. In particular embodiments, the detecting caninclude detecting a label.

In some embodiments of the above-described methods, the first sequencingreagent can include no more than two nucleotide monomers. In certainembodiments, the second sequencing reagent can include two differentnucleotide monomers which are different from the two nucleotide monomersof the first sequencing reagent.

In some embodiments of the above-described methods, the first sequencingreagent can include no more than three nucleotide monomers. In certainembodiments, the second sequencing reagent can include one nucleotidemonomer which is different from the nucleotide monomers of the firstsequencing reagent.

In other embodiments of the methods described herein, the firstsequencing reagent can include a nucleotide monomer comprising a label.In still other embodiments, the second sequencing reagent can include anucleotide monomer comprising a label. In embodiments where labels areutilized, the label can be selected from the group consisting offluorescent moieties, chromophores, antigens, dyes, phosphorescentgroups, radioactive materials, chemiluminescent moieties, scattering orfluorescent nanoparticles, Raman signal generating moieties, andelectrochemical detection moieties. Further embodiments can includecleaving the label from the nucleotide monomer.

In certain embodiments of the above-described methods, the first and/orsecond sequencing reagent can include a nucleotide monomer comprising areversibly terminating moiety. In some of these embodiments, theterminating moiety can include a reversible terminating moiety.

In embodiments where nucleotide monomers include a reversibleterminator, the method of obtaining sequence information can furtherinclude cleaving the reversible terminating moiety.

In some embodiments of the methods described herein, the firstsequencing reagent and/or the second sequencing reagent includenucleotide monomers selected from the group consisting ofdeoxyribonucleotides, modified deoxyribonucleotides, ribonucleotides,modified ribonucleotides, peptide nucleotides, modified peptidenucleotides, modified phosphate sugar backbone nucleotides and mixturesthereof.

In some embodiments of the above-described methods, the first sequencingreagent is provided to a single target nucleic acid. In otherembodiments, the first sequencing reagent can be provided simultaneouslyto a plurality of target nucleic acids. In such embodiments, theplurality of target nucleic acids can include target nucleic acidshaving different nucleotide sequences.

In certain embodiments of the above-described methods, the firstsequencing reagent can be provided to a plurality of target nucleicacids on a surface of an array in parallel. In such embodiments, theplurality of target nucleic acids can include target nucleic acidshaving the same or different nucleotide sequences.

In other embodiments, the polymerase utilized in the above-describedmethods can include a polymerase selected from the group consisting of aDNA polymerase, an RNA polymerase, a reverse transcriptase, and mixturesthereof. In still other embodiments, the polymerase can be athermostable polymerase or a thermodegradable polymerase.

Additional methods of obtaining nucleic acid sequence information caninclude the steps of (a) providing a first sequencing reagent to atarget nucleic acid in the presence of a polymerase, wherein the firstsequencing reagent comprises at least two different nucleotide monomers,and wherein the polymerase incorporates at least one nucleotide monomerof the first sequencing reagent into a polynucleotide strand, therebyproducing pyrophosphate, (b) removing at least a portion of thepyrophosphate, and (c) providing a second sequencing reagent to thetarget nucleic acid, wherein the second sequencing reagent comprises oneor more nucleotide monomers, at least one of the one or more nucleotidemonomers being different from the nucleotide monomers present in thefirst sequencing reagent, whereby sequence information for at least aportion of the target nucleic acid is obtained.

In some embodiments of the methods described herein, the at least twodifferent nucleotide monomers of the first sequencing reagent areseparately provided to the target nucleic acid.

In some embodiments of the methods described herein, the at least twodifferent nucleotide monomers of the first sequencing reagent can beprovided together to the target nucleic acid.

Other embodiments of the methods described herein can further includerepeating the method steps.

In some embodiments of the methods described herein, the polymerase canextend a polynucleotide strand. Such methods can further includedetecting the incorporation of at least one nucleotide monomer into thepolynucleotide strand. In certain embodiments, the detecting can includedetecting pyrophosphate.

In some embodiments of the above-described methods, the first sequencingreagent can include no more than two nucleotide monomers. In certainembodiments, the second sequencing reagent can include two differentnucleotide monomers which are different from the two nucleotide monomersof the first sequencing reagent.

In some embodiments of the above-described methods, the first sequencingreagent can include no more than three nucleotide monomers. In certainembodiments, the second sequencing reagent can include one nucleotidemonomer which is different from the nucleotide monomers of the firstsequencing reagent.

In some embodiments of the above-described methods, the first sequencingreagent and/or the second sequencing reagent can include nucleotidemonomers selected from the group consisting of deoxyribonucleotides,modified deoxyribonucleotides, ribonucleotides, modifiedribonucleotides, peptide nucleotides, modified peptide nucleotides,modified phosphate sugar backbone nucleotides and mixtures thereof.

In some embodiments of the above-identified methods, the firstsequencing reagent is provided to a single target nucleic acid. In otherembodiments, the first sequencing reagent is provided simultaneously toa plurality of target nucleic acids. In such embodiments, the pluralityof target nucleic acids can include target nucleic acids havingdifferent nucleotide sequences.

In certain embodiments of the methods described herein, the firstsequencing reagent is provided to a plurality of target nucleic acids ona surface of an array in parallel. In such embodiments, the plurality oftarget nucleic acids can include target nucleic acids having the same ordifferent nucleotide sequences.

In other embodiments, the polymerase utilized in the methods describedherein includes a polymerase selected from the group consisting of a DNApolymerase, an RNA polymerase, a reverse transcriptase, and mixturesthereof. In still other embodiments, the polymerase can be athermostable polymerase or a thermodegradable polymerase.

Even more methods for obtaining nucleic acid sequence information caninclude the steps of (a) detecting the incorporation of a nucleotidemonomer present in a first sequencing reagent into a polynucleotidestrand complementary to at least a portion of a target nucleic acid,wherein the first sequencing reagent comprises at least two differentnucleotide monomers, (b) removing at least a portion of the firstsequencing reagent, and (c) detecting the incorporation of a nucleotidemonomer present in a second sequencing reagent into the polynucleotidestrand, wherein the second sequencing reagent comprises one or morenucleotide monomers, at least one of the one or more nucleotide monomersbeing different from the nucleotide monomers present in the firstsequencing reagent, whereby sequence information for at least a portionof the target nucleic acid is obtained.

Other embodiments of the above-described methods, can further includerepeating the method steps.

In some embodiments of the above-described methods, the detecting caninclude detecting pyrophosphate. In particular embodiments, thedetecting can include detecting a label.

In some embodiments of the above-described methods, the first sequencingreagent can include no more than two nucleotide monomers. In certainembodiments, the second sequencing reagent can include two differentnucleotide monomers, which are different from the two nucleotidemonomers of the first sequencing reagent.

In some embodiments of the above-described methods, the first sequencingreagent includes no more than three nucleotide monomers. In certainembodiments, the second sequencing reagent can include one nucleotidemonomer, which is different from the nucleotide monomers of the firstsequencing reagent.

In other embodiments of the above-described methods, the firstsequencing reagent can include a nucleotide monomer comprising a label.In still other embodiments, the second sequencing reagent can include anucleotide monomer comprising a label. In embodiments where labels areutilized, the said label can be selected from the group consisting offluorescent moieties, chromophores, antigens, dyes, phosphorescentgroups, radioactive materials, chemiluminescent moieties, scattering orfluorescent nanoparticles, Raman signal generating moieties, andelectrochemical detection moieties. Further embodiments can includecleaving the label from the nucleotide monomer.

In certain embodiments of the above-described methods, the first and/orsecond sequencing reagent can include a nucleotide monomer comprising areversibly terminating moiety. In some of these embodiments, theterminating moiety can include a reversible terminating moiety.

In embodiments where nucleotide monomers include a reversibleterminator, the method of obtaining sequence information can furtherinclude cleaving the reversible terminating moiety.

In some embodiments of the above-described methods, the first sequencingreagent and/or the second sequencing reagent can include nucleotidemonomers selected from the group consisting of deoxyribonucleotides,modified deoxyribonucleotides, ribonucleotides, modifiedribonucleotides, peptide nucleotides, modified peptide nucleotides,modified phosphate sugar backbone nucleotides and mixtures thereof.

In some embodiments of the above-identified methods, the firstsequencing reagent is provided to a single target nucleic acid. In otherembodiments, the first sequencing reagent is provided simultaneously toa plurality of target nucleic acids. In such embodiments, the pluralityof target nucleic acids can include target nucleic acids havingdifferent nucleotide sequences.

In certain embodiments of the methods described herein, the firstsequencing reagent is provided to a plurality of target nucleic acids ona surface of an array in parallel. In such embodiments, the plurality oftarget nucleic acids can include target nucleic acids having the same ordifferent nucleotide sequences.

Some methods for obtaining nucleic acid sequence information describedherein can include the steps of (a) detecting pyrophosphate release bythe incorporation of a nucleotide monomer present in a first sequencingreagent into a polynucleotide strand complementary to at least a portionof a target nucleic acid, wherein the first sequencing reagent comprisesat least two different nucleotide monomers, (b) removing at least aportion of the pyrophosphate, and (c) detecting the incorporation of anucleotide monomer present in a second sequencing reagent into thepolynucleotide strand complementary to at least a portion of a targetnucleic acid, wherein the second sequencing reagent comprises one ormore nucleotide monomers, at least one of the one or more nucleotidemonomers being different from the nucleotide monomers present in thefirst sequencing reagent, whereby sequence information for at least aportion of the target nucleic acid is obtained.

Other embodiments of the above-described methods, can further includerepeating the method steps.

In some embodiments of the above-described methods, the first sequencingreagent can include no more than two nucleotide monomers. In certainembodiments, the second sequencing reagent can include two differentnucleotide monomers, which are different from the two nucleotidemonomers of the first sequencing reagent.

In some embodiments of the above-described methods, the first sequencingreagent includes no more than three nucleotide monomers. In certainembodiments, the second sequencing reagent can include one nucleotidemonomer, which is different from the nucleotide monomers of the firstsequencing reagent.

In some embodiments of the above-described methods, the first sequencingreagent and/or the second sequencing reagent can include nucleotidemonomers selected from the group consisting of deoxyribonucleotides,modified deoxyribonucleotides, ribonucleotides, modifiedribonucleotides, peptide nucleotides, modified peptide nucleotides,modified phosphate sugar backbone nucleotides and mixtures thereof.

In some embodiments of the above-identified methods, the firstsequencing reagent is provided to a single target nucleic acid. In otherembodiments, the first sequencing reagent is provided simultaneously toa plurality of target nucleic acids. In such embodiments, the pluralityof target nucleic acids can include target nucleic acids havingdifferent nucleotide sequences.

In certain embodiments of the methods described herein, the firstsequencing reagent is provided to a plurality of target nucleic acids ona surface of an array in parallel. In such embodiments, the plurality oftarget nucleic acids can include target nucleic acids having the same ordifferent nucleotide sequences.

Some methods for obtaining nucleic acid sequence information describedherein can include the steps of (a) detecting the incorporation of anucleotide monomer present in a first sequencing reagent into a firstpolynucleotide strand complementary to at least a portion of a targetnucleic acid, wherein the first sequencing reagent comprises at leasttwo different nucleotide monomers, (b) detecting the incorporation of anucleotide monomer present in a second sequencing reagent into the firstpolynucleotide strand, wherein the second sequencing reagent comprisesone or more nucleotide monomers, at least one of the one or morenucleotide monomers being different from the nucleotide monomers presentin the first sequencing reagent, (c) removing the first polynucleotidestrand, and (d) detecting the incorporation of a nucleotide monomerpresent in a third sequencing reagent into a second polynucleotidestrand complementary to at least a portion of the target nucleic acid,wherein the third sequencing reagent comprises two or more nucleotidemonomers, wherein at least one of the two or more nucleotide monomers isdifferent from the at least two different nucleotide monomers present inthe first sequencing reagent.

In some embodiments of the above-identified methods, the firstsequencing reagent can include no more than two nucleotide monomers. Incertain embodiments, the second sequencing reagent can include twodifferent nucleotide monomers which are different from the twonucleotide monomers of the first sequencing reagent. In furtherembodiments, the third sequencing reagent can include two nucleotidemonomers, wherein at least one of the two nucleotide monomers isdifferent from the at least two nucleotide monomers present in the firstsequencing reagent.

In some embodiments of the above-identified methods, the firstsequencing reagent can include no more than three nucleotide monomers.In certain embodiments, the second sequencing reagent can include onenucleotide monomer which is different from the nucleotide monomers ofthe first sequencing reagent. In further embodiments, the thirdsequencing reagent can include three nucleotide monomers, wherein one ofthe three nucleotide monomers is different from the at least twonucleotide monomers.

In some embodiments of the above-identified methods, the firstsequencing reagent can include a nucleotide monomer comprising a label.In still other embodiments, the second sequencing reagent can include anucleotide monomer comprising a label. In yet other embodiments, thethird sequencing reagent can include a nucleotide monomer comprising alabel. In embodiments where labels are utilized, the label can beselected from the group consisting of fluorescent moieties,chromophores, antigens, dyes, phosphorescent groups, radioactivematerials, chemiluminescent moieties, scattering or fluorescentnanoparticles, Raman signal generating moieties, and electrochemicaldetection moieties. Further embodiments can include cleaving the labelfrom the nucleotide monomer.

In certain embodiments of the above-described methods, the first and/orsecond sequencing reagent can include a nucleotide monomer comprising areversibly terminating moiety. In some of these embodiments, theterminating moiety can include a reversible terminating moiety.

In embodiments where nucleotide monomers include a reversibleterminator, the method of obtaining sequence information can furtherinclude cleaving the reversible terminating moiety.

In some embodiments of the above-identified methods, the firstsequencing reagent, the second sequencing reagent and/or the thirdsequencing reagent can include nucleotide monomers selected from thegroup consisting of deoxyribonucleotides, modified deoxyribonucleotides,ribonucleotides, modified ribonucleotides, peptide nucleotides, modifiedpeptide nucleotides, modified phosphate sugar backbone nucleotides andmixtures thereof.

In some embodiments of the above-identified methods, the firstsequencing reagent is provided to a single target nucleic acid. In otherembodiments, the first sequencing reagent is provided simultaneously toa plurality of target nucleic acids. In such embodiments, the pluralityof target nucleic acids can include target nucleic acids havingdifferent nucleotide sequences.

In certain embodiments of the methods described herein, the firstsequencing reagent is provided to a plurality of target nucleic acids ona surface of an array in parallel. In such embodiments, the plurality oftarget nucleic acids can include target nucleic acids having the same ordifferent nucleotide sequences.

Additional methods for obtaining nucleic acid sequence information caninclude the steps of (a) providing a first low resolution sequencerepresentation for a target nucleic acid, wherein the first lowresolution sequence representation is degenerate with respect to two ormore nucleotide types, (b) providing a second low resolution sequencerepresentation for the target nucleic acid, wherein the second lowresolution sequence representation is degenerate with respect to two ormore nucleotide types, wherein at least one of the two or morenucleotide types in the first low resolution sequence representation isdifferent from at least one of the two or more nucleotide types in thesecond low resolution sequence representation, and (c) comparing thefirst low resolution sequence representation and the second lowresolution sequence representation to determine the actual sequence ofthe target nucleic acid at single nucleotide resolution.

In some embodiments of the above-described methods, the method can becarried out by a computer. For example, the low resolution sequencerepresentations can be provided to a computer that is programmed tocompare the representations to determine the actual sequence of thetarget nucleic acid at single nucleotide resolution. The computer can befurther programmed to store one or more of the representations and theactual sequence. The computer can be programmed to transmit one or moreof the representations and the actual sequence to a user, to anothercomputer or to a network.

In particular embodiments of the above-described methods, the first lowresolution sequence representation can be degenerate with respect to apair of nucleotide types.

In certain embodiments, the first low resolution sequence representationcan be degenerate with respect to two pairs of nucleotide types. Forexample, the first low resolution sequence representation can bedegenerate with respect to A and T at particular positions in the actualsequence of the target nucleic acid and the first low resolutionsequence representation can be degenerate with respect to G and C atparticular positions in the actual sequence of the target nucleic acid.Continuing with the example, the second low resolution sequencerepresentation can be degenerate with respect to A and C at particularpositions in the actual sequence of the target nucleic acid and thesecond low resolution sequence representation can be degenerate withrespect to G and T at particular positions in the actual sequence of thetarget nucleic acid. Alternatively, the second low resolution sequencerepresentation can be degenerate with respect to A and G at particularpositions in the actual sequence of the target nucleic acid and thesecond low resolution sequence representation can be degenerate withrespect to C and T at particular positions in the actual sequence of thetarget nucleic acid.

In some embodiments of the above-described methods, the first lowresolution sequence representation can be degenerate with respect to atriplet of nucleotide types.

In particular embodiments of the above-described methods, the first lowresolution sequence representation can include a string of symbols andthe number of different symbol types in the string can be less than thenumber of different nucleotide types in the actual sequence of thenucleic acid.

One or more low resolution sequence representations used in a method setforth above can be obtained from a sequencing reaction that includes therepeated steps of (i) detecting the incorporation of a first sequencingreagent into a polynucleotide strand complementary to at least a portionof the target nucleic acid, wherein said first sequencing reagentcomprises at least two different nucleotide monomers, and (ii) detectingthe incorporation of a second sequencing reagent into the polynucleotidestrand, wherein said second sequencing reagent comprises one or morenucleotide monomers, at least one of said one or more nucleotidemonomers being different from the nucleotide monomers present in saidfirst sequencing reagent.

In particular embodiments of the methods set forth above, patternrecognition methods can be used to determine the actual sequence of atarget nucleic acid at single nucleotide resolution.

A comparing step of a method set forth above, can be carried out byalignment of the first low resolution sequence representation and thesecond low resolution sequence to reference sequences in a database,wherein the reference sequences include the actual sequence of thetarget nucleic acid.

Also provided are methods for determining the presence or absence of atarget nucleic acid. Such methods can include the steps of (a) providinga first low resolution sequence representation for a target nucleicacid, wherein the target nucleic acid is obtained from a target sample,wherein the first low resolution sequence representation is degeneratewith respect to two or more nucleotide types, (b) providing a second lowresolution sequence representation for the target nucleic acid, whereinthe target nucleic acid is obtained from a reference sample, wherein thesecond low resolution sequence representation is degenerate with respectto two or more nucleotide types, and (c) comparing the first lowresolution sequence representation and the second low resolutionsequence representation to determine the presence or absence of thetarget nucleic acid in the target sample.

In particular embodiments of the above-described methods, the two ormore nucleotide types in the first low resolution sequencerepresentation are the same as the two or more nucleotide types in thesecond low resolution sequence representation,

In some embodiments of the above-described methods, a first plurality oflow resolution sequence representations for a plurality of nucleic acidsin the target sample are provided and a second plurality of lowresolution sequence representations for a plurality of nucleic acids inthe reference sample are provided. Furthermore, the first low resolutionsequence representation for the target nucleic acid and the second lowresolution sequence representation for the target nucleic acid can bedistinguished from low resolution sequence representations in the firstplurality and in the second plurality.

Embodiments of the above-described methods can further includequantifying the amount of the target nucleic acid in the target samplerelative to the amount of the target nucleic acid in the referencesample. For example, the target nucleic acid can be an mRNA and theamount can be indicative of an expression level for the mRNA.

In particular embodiments of the above-described methods, the first andsecond low resolution sequence representations have a known correlationwith the actual sequence of the target nucleic acid at single nucleotideresolution.

In some embodiments of the above-described methods, the first lowresolution sequence representation and the second low resolutionsequence representation are the same.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graph depicting the length of base pair reads for single,doublet, and triplet delivery methods.

FIG. 2 is a diagram showing a doublet delivery and sequencedetermination scheme. In a first round of doublet sequencing on a targetsequence (SEQ ID NO: 01), a 1^(st) predicted sequence (SEQ ID NO: 02)can be obtained. In a second round of doublet sequencing on the targetsequence (SEQ ID NO: 01), a 2^(nd) predicted sequence (SEQ ID NO: 03)can be obtained. The 1^(st) and 2^(nd) predicted sequences can becombined to show the sequence of the target sequence (SEQ ID NO: 01).

DETAILED DESCRIPTION

The present technology relates to methods for sequencing polymers suchas nucleic acids. Some embodiments relate to sequencing-by-synthesis(SBS) methodologies. Particular embodiments relate to extending the readlength produced by SBS and other sequencing methods.

Generally, SBS techniques include the enzymatic extension of a nascentpolynucleotide strand complementary to a target nucleic acid templatethrough the iterative addition of nucleotide monomers and determiningthe sequence of the target nucleic acid template based on the order ofaddition for the nucleotide monomers. In some SBS methods, eachnucleotide monomer addition to a nascent polynucleotide can occur in adelivery step. Distinct delivery steps are repeated for each nucleotide,for example, dATP, dCTP, dGTP, and dTTP in a round of sequencing. Insuch SBS chemistries, the total number of deliveries can determine, inpart, the upper limit of a particular read length in a sequencing run.However, without wishing to be bound to any theory, it is believed thatparticular non idealities, for example, properties of the nucleic acidsbeing sequenced, such as presence of homopolymer sequence stretches; ormanipulations involved in SBS chemistry, such as photooxidation ofnucleic acids and other reagents due to irradiation with light; orchemical degradation due to contaminants in reagents, can result insignificantly shorter read lengths than anticipated. In some instances,an average read length may be less than 60% of the number of nucleotidedeliveries. Although the invention is exemplified herein using SBSmethods of nucleic acid sequencing, the principles can be extended toother sequencing methods whether applied to nucleic acids or otherpolymers.

DEFINITIONS

As used herein, “a sequencing reagent” and grammatical equivalentsthereof can refer to a composition, such as a solution, comprising oneor more monomeric precursors of a polymer such as nucleotide monomers.In some embodiments, a sequencing reagent includes one or morenucleotide monomers having a label moiety, a terminator moiety, or both.Such moieties are chemical groups that are not naturally occurringmoieties of nucleic acids, being introduced by synthetic means to alterthe natural characteristics of the nucleotide monomers with regard todetectability under particular conditions or enzymatic reactivity underparticular conditions. Alternatively, a sequencing reagent comprises oneor more nucleotide monomers that lack a label moiety and/or a terminatormoiety. In some embodiments, the sequencing reagent consists of oressentially consists of one nucleotide monomer, two different nucleotidemonomers, three different nucleotide monomers or four differentnucleotide monomers. It should be understood that when providing asequencing reagent comprising multiple nucleotide monomers to a targetnucleic acid, the nucleotide monomers do not necessarily have to beprovided at the same time. However, in preferred embodiments of themethods described herein, multiple nucleotide monomers are providedtogether (at the same time) to the target nucleic acid. Irrespective ofwhether the multiple nucleotide monomers are provided to the targetnucleic acid separately or together, the result is that the sequencingreagent, including the nucleotide monomers contained therein, aresimultaneously in the presence of the target nucleic acid. For example,two nucleotide monomers can be delivered, either together or separately,to a target nucleic acid. In such embodiments, a sequencing reagentcomprising two nucleotide monomers will have been provided to the targetnucleic acid. In some embodiments, zero, one or two of the nucleotidemonomers will be incorporated into a polynucleotide that iscomplementary to the target nucleic acid.

As used here, “complementary polynucleotides” includes polynucleotidestrands that are not necessarily complementary to the full length of thetarget sequence. That is, a complementary polynucleotide can becomplementary to only a portion of the target nucleic acid. As morenucleotide monomers are incorporated into the complementarypolynucleotide, the complementary polynucleotide becomes complementaryto a greater portion of the target nucleic acid. Typically, thecomplementary portion is a contiguous portion of the target nucleicacid.

As used herein, “a round of sequencing” or “a sequencing run” and/orgrammatical variants thereof can refer to a repetitive process ofphysical or chemical steps that is carried out to obtain signalsindicative of the order of monomers in a polymer. For example, the stepscan be initiated on a nucleic acid target and carried out to obtainsignals indicative of the order of bases in the nucleic acid target. Theprocess can be carried out to its typical completion, which is usuallydefined by the point at which signals from the process can no longerdistinguish bases of the target with a reasonable level of certainty. Ifdesired, completion can occur earlier, for example, once a desiredamount of sequence information has been obtained. A sequencing run canbe carried out on a single target nucleic acid molecule orsimultaneously on a population of target nucleic acid molecules havingthe same sequence, or simultaneously on a population of target nucleicacids having different sequences. In some embodiments, a sequencing runis terminated when signals are no longer obtained from one or moretarget nucleic acid molecules from which signal acquisition wasinitiated. For example, a sequencing run can be initiated for one ormore target nucleic acid molecules that are present on a solid phasesubstrate and terminated upon removal of the one or more target nucleicacid molecules from the substrate or otherwise ceasing detection of thetarget nucleic acids that were present on the substrate when thesequencing run was initiated.

As used herein, “cycle” and/or grammatical variants thereof can refer tothe portion of a sequencing run that is repeated to indicate thepresence of at least one monomer in a polymer. Typically, a cycleincludes several steps such as steps for delivery of reagents, washingaway unreacted reagents and detection of signals indicative of changesoccurring in response to added reagents. For example, a cycle of an SBSreaction can include delivery of a sequencing reagent that includes oneor more type of nucleotide, washing to remove unreacted nucleotides, anddetection to detect one or more nucleotides that are incorporated in anextended nucleic acid.

As used herein, “flow step” and/or “delivery” and grammaticalequivalents thereof can refer to providing a sequencing reagent to atarget polymer such as a target nucleic acid. In some embodiments, thesequencing reagent contains one or more nucleotide monomers. Flow stepsor deliveries can be repeated in multiple cycles in a round ofsequencing.

As used herein, “nucleotide monomer” and grammatical equivalents thereofcan refer to a nucleotide or nucleotide analog that can becomeincorporated into a polynucleotide. In the methods described herein, thenucleotide monomers are separate non-linked nucleotides. That is, thenucleotide monomers are not present as dimers, trimers, etc. Suchnucleotide monomers may be substrates for an enzyme that may extend apolynucleotide strand. Nucleotide monomers may or may not becomeincorporated into a nascent polynucleotide in a flow step. Examples ofnucleotide monomers include deoxyribonucleotides, modifieddeoxyribonucleotides, ribonucleotides, modified ribonucleotides, peptidenucleotides, modified peptide nucleotides, modified phosphate sugarbackbone nucleotides and mixtures thereof. Nucleotide analogs whichinclude a modified nucleobase can also be used in the methods describedherein. As is known in the art, certain nucleotide analogues cannotbecome incorporated into a polynucleotide, for example, nucleotideanalogues such as adenosine 5′ phosphosulfate.

Aspects of the methods described herein can include removing at least aportion of a substance from a site of activity. Such sites of activitycan include sites of incorporation and/or detection. For example, asubstance may be removed from the site of incorporation or the presenceof a polymerase. Methods of removing a substance from a site of activitycan include for example, washing the substance from the site,sequestering the substance from the site of activity, and degrading thesubstance.

As used herein, “a portion” and “at least a portion” and grammaticalequivalents thereof can refer to any fraction of a whole amount. In someembodiments, “at least a portion” refers to at least about 10%, 20%,30%, 40%, 50%, 60%, 70%, 80%, 90% and 100% of a whole amount.

As used herein, “sequence representation” and grammatical equivalentsthereof, when used in reference to a polymer, can refer to informationthat signifies the order and type of monomeric units in the polymer. Forexample, the information can indicate the order and type of nucleotidesin a nucleic acid. The information can be in any of a variety of formatsincluding, for example, a depiction, image, electronic medium, series ofsymbols, series of numbers, series of letters, series of colors, etc.The information can be at single monomer resolution or at lowerresolution, as set forth in further detail below. An exemplary polymeris a nucleic acid, such as DNA or RNA, having nucleotide units. A seriesof “A,” “T,” “G,” and “C” letters is a well known sequencerepresentation for DNA that can be correlated, at single nucleotideresolution, with the actual sequence of a DNA molecule. Other exemplarypolymers are proteins having amino acid units and polysaccharides havingsaccharide units.

As used herein, “low resolution” and grammatical equivalents thereof,when used in reference to a sequence representation, can refer to aresolution at which at least a one type of monomeric unit in a polymercan be distinguished from at least a first other type of monomeric unitin the polymer, but cannot necessarily be distinguished from a secondother type of monomeric unit in the polymer. For example, low resolutionwhen used in reference to a sequence representation of a nucleic acidmeans that two or three of four possible nucleotide types can beindicated as candidate residents at a particular position in thesequence while the two or three nucleotide types cannot necessarilybeing distinguished from each other in the sequence representation. Inparticular embodiments, two different monomeric units from an actualpolymer sequence can be assigned a common label or identifier in a lowresolution sequence representation. In some embodiments, three differentmonomeric units from an actual polymer sequence can be assigned a commonlabel or identifier in a low resolution sequence representation.Typically, the diversity of different characters in a low resolutionsequence representation will be fewer than the diversity of differenttypes of monomers in the polymer represented by the low resolutionsequence representation. For example, a low resolution representation ofa nucleic acid can include a string of symbols and the number ofdifferent symbol types in the string can be less than the number ofdifferent nucleotide types in the actual sequence of the nucleic acid.

As used herein “position” and grammatical equivalents thereof, when usedin reference to a sequence, can refer to the location of a unit in thesequence. The location can be identified, for example, relative to otherlocations in the same sequence. Alternatively or additionally, thelocation can be identified with reference to another sequence or series.Although one or more characteristic of the unit may be known, any suchcharacteristics need not be considered in identifying position.

As used herein, “degenerate” and grammatical equivalents thereof canrefer to having more than one state or identification. When used inreference to a nucleic acid representation, the term refers to aposition in the nucleic acid representation for which two or morenucleotide types are identified as candidate occupants in thecorresponding position of the actual nucleic acid sequence. A degenerateposition in a nucleic acid can have, for example, 2, 3 or 4 nucleotidetypes as candidate occupants. In particular embodiments, the number ofdifferent nucleotide types at a degenerate position in a sequencerepresentation can be greater than one and less than three (i.e. two).In other embodiments, the number of different nucleotide types at adegenerate position in a sequence representation can be greater than oneand less than four (i.e. two or three). Typically, the number ofdifferent nucleotide types at a degenerate position in a sequencerepresentation can be less than the number of different nucleotide typespresent in the actual nucleic acid sequence that is represented.

Aspects of the current disclosure describe methods for extending thelength of nucleic acid sequence reads obtained by sequencingmethodologies. In some methods described herein, a sequencing reagentcan be provided to a target nucleic acid in a single delivery in whichthe sequencing reagent comprises two or more different nucleotidemonomers. At each delivery, two or more types of nucleotide monomer canbe incorporated into a polynucleotide. Using such methods, long readlengths can be achieved because for any given cycle the polynucleotidecan be extended by multiple nucleotides, whereas single nucleotidedelivery methods might only yield multiple incorporations for regions ofa template that are homopolymeric. Although a single sequencing runusing only multiple nucleotide monomer delivery would typically providea lower resolution than methods where one type of nucleotide monomer isprovided at each delivery, resolutions at least on par with singlenucleotide monomer delivery can be achieved by performing a secondsequencing run using a doublet combination different from the doubletcombination used in the first run. The difference between runs performedusing multiple nucleotide monomer delivery as compared to singlenucleotide delivery, however, is that the read length of the sequenceobtained by multiple nucleotide monomer delivery can be significantlylonger than the read length of a the sequence obtained by singlenucleotide monomer delivery. Furthermore, as discussed in detail herein,there are several applications for lower resolution sequence obtained bysingle runs using multiple nucleotide monomer delivery.

In an exemplary embodiment, a doublet delivery method can be used. Insuch an embodiment, a sequencing reagent comprising two types ofnucleotide monomer, for example, dATP and dCTP, can be provided in afirst delivery to a target nucleic acid in the presence of polymerase.In the subsequent delivery, a sequencing reagent comprising two types ofnucleotide monomers different from the nucleotide monomers of theprevious delivery, for example, dGTP and dTTP can be provided to thetarget nucleic acid. The deliveries can be repeated and sequenceinformation of the target nucleic acid can be obtained. In someembodiments, doublet delivery methods can provide sequence read lengthsof at least 1.8 times the number of total deliveries (FIG. 1). This isin contrast to methods where single nucleotide monomers are provided ineach delivery. In such methods, the typical read length is substantiallyless than the number of deliveries (FIG. 1).

In some doublet delivery methods, there can be three doublet deliverycombinations that can be used, for example, dATP/dCTP+dGTP/dTTP;dATP/dGTP+dCTP/dTTP; and dATP/dTTP+dCTP/dGTP ([First delivery nucleotidemonomers]+[Second delivery nucleotide monomers]).

It is contemplated that in some embodiments, a target nucleic acid mayundergo at least two rounds of sequencing. For example, a first roundmay use one doublet delivery combination, and a second round may use adifferent doublet delivery combination. On combining the sequence dataobtained from each round of sequencing, such embodiments can providesequence information of a target nucleic acid at single-base resolution(Example 2, and FIG. 2).

Doublet delivery methods are also contemplated where a target nucleicacid can undergo three rounds of sequencing in which each doubletdelivery combination is used. On combining the sequence data obtainedfrom each round of sequencing, sequence information of the targetnucleic acid can be obtained at single-base resolution with additionalerror checking.

In addition to doublet delivery methods, triplet delivery methods arealso contemplated. Using such methods, a round of sequencing can beperformed in which three different nucleotide monomers can be providedto a target nucleic acid in a delivery. In the next delivery, anucleotide monomer which is different from the three nucleotide monomersof the previous delivery can be provided to the target nucleic acid. Thecombination of deliveries can be repeated for a round of sequencing andsequence information of the target nucleic acid can be obtained. In someembodiments, read lengths of at least 3 times the number of totaldeliveries can be readily achieved (FIG. 1).

In another embodiment of triplet delivery methods, a round of sequencingcan be performed in which three different nucleotide monomers can beprovided to a target nucleic acid in a delivery. In the next delivery, aplurality of nucleotide monomers, wherein at least one of the nucleotidemonomers is different from each of the nucleotide monomers of the priordelivery can be provided to the target nucleic acid. This combination ofdeliveries can be repeated for a round of sequencing and sequenceinformation of the target nucleic acid can be obtained. As discussedabove, triplet delivery methods followed by delivery of a singlenucleotide monomer that is different from each of the previouslyprovided nucleotide monomers can produce sequence information relatingto the position of a particular nucleotide monomer

It will be appreciated that other combinations of nucleotide deliveriesusing nucleotide monomers can be used provided that the nucleotidemonomers permit extension of a polynucleotide complementary to thetarget nucleic acid so as to obtain sequencing data. For example, themethods can employ a combination of several triplet deliveries, acombination of doublet and triplet deliveries, or a combination ofsinglet, doublet and triplet deliveries.

As will be apparent to the skilled artisan, the methods described hereinhave several significant applications. For example, methods describedherein can be used to obtain long lengths of nucleic acid sequence at alow resolution and/or high resolution.

Methods to obtain long read lengths of sequence are an important tool inde novo genome sequencing. Sequencing massive lengths of genomic nucleicacids often requires the assembly of many shorter overlapping fragmentsof sequence into contigs. Difficulties in contig assembly can arise whenshort length reads of long homopolymer stretches of sequence must beassembled because it is difficult to accurately produce the homopolymerregion from short sequences within the homopolymer region. Increasingthe length of a contiguous sequencing read greatly reduces this problemby increasing the likelihood of producing fragments with sufficientsequence variation to permit homopolymer regions to be accuratelyassembled. Furthermore, long read lengths of sequence can providescaffolds for the assembly of shorter fragments of sequence, obviatingthe need for many smaller sequences to contain overlapping sequences.

In addition, the long read lengths that can be obtained using themethods described herein can be used as a molecular DNA signature forapplications involved in genotyping, expression profiling, for example,capturing alternative splicing, genome mapping, amplicon sequencing, andmetagenomics.

It will be appreciated that in any of the methods described herein theorder of sequencing reagent addition can be reversed. For example, intriplet delivery methods, a single nucleotide monomer can be provided inthe first delivery of sequencing reagent. In the next delivery, thesecond sequencing reagent can comprise three nucleotide monomers thatare different from the nucleotide monomer in the first sequencingreagent.

Furthermore, in some embodiments of the methods described herein, afirst sequencing reagent can provide at least one type of nucleotidemonomer. In such embodiments, a second sequencing reagent can contain atleast two different nucleotide monomers. At least one of the at leasttwo different nucleotide monomers of the second sequencing reagent canbe different from the nucleotide monomer of the first sequencingreagent. In an exemplary embodiment, the first sequencing reagent cancontain a single nucleotide monomer, for example, dATP, and the secondsequencing reagent can contain three nucleotide monomers, for example,dCTP, dGTP, and dTTP.

Alternatively, other delivery combinations can be used. For example, afirst sequencing reagent comprising one nucleotide monomer, followed bya second sequencing reagent comprising two of four different nucleotidemonomers, followed by a third sequencing reagent comprising theremaining two of the four different nucleotide monomers is contemplated.As for other embodiments, the temporal order of additions is exemplaryand other orders for delivering various combinations of nucleotides arealso contemplated.

Target Nucleic Acids

A target nucleic acid can include any nucleic acid of interest. Targetnucleic acids can include, but are not limited to, DNA, RNA, peptidenucleic acid, morpholino nucleic acid, locked nucleic acid, glycolnucleic acid, threose nucleic acid, mixtures thereof, and hybridsthereof. In a preferred embodiment, genomic DNA fragments or amplifiedcopies thereof are used as the target nucleic acid. In another preferredembodiment, mitochondrial or chloroplast DNA is used.

A target nucleic acid can comprise any nucleotide sequence. In someembodiment, the target nucleic acid comprises homopolymer sequences. Atarget nucleic acid can also include repeat sequences. Repeat sequencescan be any of a variety of lengths including, for example, 2, 5, 10, 20,30, 40, 50, 100, 250, 500, 1000 nucleotides or more. Repeat sequencescan be repeated, either contiguously or non-contiguously, any of avariety of times including, for example, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15,20 times or more.

Some embodiments can utilize a single target nucleic acid. Otherembodiments can utilize a plurality of target nucleic acids. In suchembodiments, a plurality of target nucleic acids can include a pluralityof the same target nucleic acids, a plurality of different targetnucleic acids where some target nucleic acids are the same, or aplurality of target nucleic acids where all target nucleic acids aredifferent. Embodiments that utilize a plurality of target nucleic acidscan be carried out in multiplex formats such that reagents are deliveredsimultaneously to the target nucleic acids, for example, in a singlechamber or on an array surface. In preferred embodiments, target nucleicacids can be amplified as described in more detail herein. In someembodiments, the plurality of target nucleic acids can includesubstantially all of a particular organism's genome. The plurality oftarget nucleic acids can include at least a portion of a particularorganism's genome including, for example, at least about 1%, 5%, 10%,25%, 50%, 75%, 80%, 85%, 90%, 95%, or 99% of the genome. In particularembodiments the portion can have an upper limit that is at most about1%, 5%, 10%, 25%, 50%, 75%, 80%, 85%, 90%, 95%, or 99% of the genome

Target nucleic acids can be obtained from any source. For example,target nucleic acids may be prepared from nucleic acid moleculesobtained from a single organism or from populations of nucleic acidmolecules obtained from natural sources that include one or moreorganisms. Sources of nucleic acid molecules include, but are notlimited to, organelles, cells, tissues, organs, or organisms. Cells thatmay be used as sources of target nucleic acid molecules may beprokaryotic (bacterial cells, for example, Escherichia, Bacillus,Serratia, Salmonella, Staphylococcus, Streptococcus, Clostridium,Chlamydia, Neisseria, Treponema, Mycoplasma, Borrelia, Legionella,Pseudomonas, Mycobacterium, Helicobacter, Erwinia, Agrobacterium,Rhizobium, and Streptomyces genera); archeaon, such as crenarchaeota,nanoarchaeota or euryarchaeotia; or eukaryotic such as fungi, (forexample, yeasts), plants, protozoans and other parasites, and animals(including insects (for example, Drosophila spp.), nematodes (forexample, Caenorhabditis elegans), and mammals (for example, rat, mouse,monkey, non-human primate and human)).

Polymerases

The methods described herein can utilize polymerases. For example,polymerases can include, but are not limited to, DNA polymerases, RNApolymerases, reverse transcriptases, and mixtures thereof. Thepolymerase can be a thermostable polymerase or a thermodegradablepolymerase. Examples of thermostable polymerases include polymerasesisolated from Thermus aquaticus, Thermus thermophilus, Pyrococcuswoesei, Pyrococcus furiosus, Thermococcus litoralis, Bacillusstearothermophilus, and Thermotoga maritima. Examples ofthermodegradable polymerases include E. coli DNA polymerase, the Klenowfragment of E. coli DNA polymerase, T4 DNA polymerase, and T7 DNApolymerase. More examples of polymerases that can be used with themethods described herein include E. coli, T7, T3, and SP6 RNApolymerases, and AMV, M-MLV, and HIV reverse transcriptases. In someembodiments, the polymerase can have proofreading activity or otherenzymic activities. Polymerases can also be engineered for example, toenhance or modify reactivity with various nucleotide analogs or toreduce an activity such as proofreading or exonuclease activity.

Sequencing Methods

The methods described herein can be used in conjunction with a varietyof sequencing techniques. In some embodiments, the process to determinethe nucleotide sequence of a target nucleic acid can be an automatedprocess. Preferred embodiments include SBS techniques.

SBS techniques generally involve the enzymatic extension of a nascentnucleic acid strand through the iterative addition of nucleotidesagainst a template strand. In traditional methods of SBS, a singlenucleotide monomer may be provided to a target nucleotide in thepresence of a polymerase in each delivery. However, in the methodsdescribed herein, more than one type of nucleotide monomer can beprovided to a target nucleic acid in the presence of a polymerase in adelivery.

SBS can utilize nucleotide monomers that have a terminator moiety orthose that lack any terminator moieties. Methods utilizing nucleotidemonomers lacking terminators include, for example, pyrosequencing andsequencing using γ-phosphate-labeled nucleotides, as set forth infurther detail below. In methods using nucleotide monomers lackingterminators, the number of nucleotides added in each cycle is generallyvariable and dependent upon the template sequence and the mode ofnucleotide delivery. For SBS techniques that utilize nucleotide monomershaving a terminator moiety, the terminator can be effectivelyirreversible under the sequencing conditions used as is the case fortraditional Sanger sequencing which utilizes dideoxynucleotides, or theterminator can be reversible as is the case for sequencing methodsdeveloped by Solexa (now Illumina, Inc.).

SBS techniques can utilize nucleotide monomers that have a label moietyor those that lack a label moiety. Accordingly, incorporation events canbe detected based on a characteristic of the label, such as fluorescenceof the label; a characteristic of the nucleotide monomer such asmolecular weight or charge; a byproduct of incorporation of thenucleotide, such as release of pyrophosphate; or the like. Inembodiments, where two or more different nucleotides are present in asequencing reagent, the different nucleotides can be distinguishablefrom each other, or alternatively, the two or more different labels canbe the indistinguishable under the detection techniques being used. Forexample, the different nucleotides present in a sequencing reagent canhave different labels and they can be distinguished using appropriateoptics as exemplified by the sequencing methods developed by Solexa (nowIllumina, Inc.). However, it is also possible to use the same label forthe two or more different nucleotides present in a sequencing reagent orto use detection optics that do not necessarily distinguish thedifferent labels. Thus, in a doublet sequencing reagent having a mixtureof dATP/dCTP both the dATP and dCTP can be labeled with the samefluorophore. Furthermore, when doublet delivery methods are used all ofthe different nucleotide monomers can have the same label or differentlabels can be used, for example, to distinguish one mixture of differentnucleotide monomers from a second mixture of nucleotide monomers. Forexample, using the [First delivery nucleotide monomers]+[Second deliverynucleotide monomers] nomenclature set forth above and taking an exampleof dATP/dCTP+dGTP/dTTP, the dATP and dCTP monomers can have the samefirst label and the dGTP and dTTP monomers can have the same secondlabel, wherein the first label is different from the second label.Alternatively, the first label can be the same as the second label andincorporation events of the first delivery can be distinguished fromincorporation events of the second delivery based on the temporalseparation of cycles in an SBS protocol. Accordingly, a low resolutionsequence representation obtained from such mixtures will be degeneratefor two pairs of nucleotides (T/G, which is complementary to A and C,respectively; and C/A which is complementary to G/T, respectively).

Preferred embodiments include pyrosequencing techniques. Pyrosequencingdetects the release of inorganic pyrophosphate (PPi) as particularnucleotides are incorporated into the nascent strand (Ronaghi, M.,Karamohamed, S., Pettersson, B., Uhlen, M. and Nyren, P. (1996)“Real-time DNA sequencing using detection of pyrophosphate release.”Analytical Biochemistry 242(1), 84-9; Ronaghi, M. (2001) “Pyrosequencingsheds light on DNA sequencing.” Genome Res. 11(1), 3-11; Ronaghi, M.,Uhlen, M. and Nyren, P. (1998) “A sequencing method based on real-timepyrophosphate.” Science 281(5375), 363; U.S. Pat. No. 6,210,891; U.S.Pat. No. 6,258,568 and U.S. Pat. No. 6,274,320, the disclosures of whichare incorporated herein by reference in their entireties). Inpyrosequencing, released PPi can be detected by being immediatelyconverted to adenosine triphosphate (ATP) by ATP sulfurylase, and thelevel of ATP generated is detected via luciferase-produced photons.

In another exemplary type of SBS, cycle sequencing is accomplished bystepwise addition of reversible terminator nucleotides containing, forexample, a cleavable or photobleachable dye label as described, forexample, in WO 04/018497 and U.S. Pat. No. 7,057,026, the disclosures ofwhich are incorporated herein by reference. This approach is beingcommercialized by Solexa (now Illumina Inc.), and is also described inWO 91/06678 and WO 07/123,744, each of which is incorporated herein byreference. The availability of fluorescently-labeled terminators inwhich both the termination can be reversed and the fluorescent labelcleaved facilitates efficient cyclic reversible termination (CRT)sequencing. Polymerases can also be co-engineered to efficientlyincorporate and extend from these modified nucleotides.

In accordance with the methods set forth herein, the two or moredifferent nucleotide monomers that are present in a sequencing reagentor delivered to a template nucleic acid in the same cycle of asequencing run need not have a terminator moiety. Rather, as is the casewith pyrosequencing, several of the nucleotide monomers can be added toa primer in a template directed fashion without the need for anintermediate deblocking step. The nucleotide monomers can contain labelsfor detection, such as fluorescent labels, and can be used in methodsand instruments similar to those commercialized by Solexa (now IlluminaInc.). Preferably in such embodiments, the labels do not substantiallyinhibit extension under SBS reaction conditions. However, the detectionlabels can be removable, for example, by cleavage or degradation.Removal of the labels after they have been detected in a particularcycle and prior to a subsequent cycle can provide the advantage ofreducing background signal and crosstalk between cycles. Examples ofuseful labels and removal methods are set forth below.

In particular embodiments some or all of the nucleotide monomers caninclude reversible terminators. In such embodiments, reversibleterminators/cleavable fluors can include fluor linked to the ribosemoiety via a 3′ ester linkage (Metzker, Genome Res. 15:1767-1776 (2005),which is incorporated herein by reference). Other approaches haveseparated the terminator chemistry from the cleavage of the fluorescencelabel (Ruparel et al., Proc Natl Acad Sci USA 102: 5932-7 (2005), whichis incorporated herein by reference in its entirety). Ruparel et aldescribed the development of reversible terminators that used a small 3′allyl group to block extension, but could easily be deblocked by a shorttreatment with a palladium catalyst. The fluorophore was attached to thebase via a photocleavable linker that could easily be cleaved by a 30second exposure to long wavelength UV light. Thus, either disulfidereduction or photocleavage can be used as a cleavable linker. Anotherapproach to reversible termination is the use of natural terminationthat ensues after placement of a bulky dye on a dNTP. The presence of acharged bulky dye on the dNTP can act as an effective terminator throughsteric and/or electrostatic hindrance. The presence of one incorporationevent prevents further incorporations unless the dye is removed.Cleavage of the dye removes the fluor and effectively reverses thetermination. Examples of modified nucleotides are also described in U.S.Pat. No. 7,427,673, and U.S. Pat. No. 7,057,026, the disclosures ofwhich are incorporated herein by reference in their entireties.

Additional exemplary SBS systems and methods which can be utilized withthe methods and systems described herein are described in U.S. PatentApplication Publication No. 2007/0166705, U.S. Patent ApplicationPublication No. 2006/0188901, U.S. Pat. No. 7,057,026, U.S. PatentApplication Publication No. 2006/0240439, U.S. Patent ApplicationPublication No. 2006/0281109, PCT Publication No. WO 05/065814, U.S.Patent Application Publication No. 2005/0100900, PCT Publication No. WO06/064199 and PCT Publication No. WO 07/010,251, the disclosures ofwhich are incorporated herein by reference in their entireties.

Some embodiments can utilize sequencing by ligation techniques. Suchtechniques utilize DNA ligase to incorporate nucleotides and identifythe incorporation of such nucleotides. Exemplary SBS systems and methodswhich can be utilized with the methods and systems described herein aredescribed in U.S. Pat. No. 6,969,488, U.S. Pat. No. 6,172,218, and U.S.Pat. No. 6,306,597, the disclosures of which are incorporated herein byreference in their entireties.

Some embodiments can utilize nanopore sequencing (Deamer, D. W. &Akeson, M. “Nanopores and nucleic acids: prospects for ultrarapidsequencing.” Trends Biotechnol. 18, 147-151 (2000); Deamer, D. and D.Branton, “Characterization of nucleic acids by nanopore analysis”. Acc.Chem. Res. 35:817-825 (2002); Li, J., M. Gershow, D. Stein, E. Brandin,and J. A. Golovchenko, “DNA molecules and configurations in asolid-state nanopore microscope” Nat. Mater. 2:611-615 (2003), thedisclosures of which are incorporated herein by reference in theirentireties). In such embodiments, the target nucleic acid passes througha nanopore. The nanopore can be a synthetic pore or biological membraneprotein, such as α-hemolysin. As the target nucleic acid passes throughthe nanopore, each base-pair can be identified by measuring fluctuationsin the electrical conductance of the pore. (U.S. Pat. No. 7,001,792;Soni, G. V. & Meller, “A. Progress toward ultrafast DNA sequencing usingsolid-state nanopores.” Clin. Chem. 53, 1996-2001 (2007); Healy, K.“Nanopore-based single-molecule DNA analysis.” Nanomed. 2, 459-481(2007); Cockroft, S. L., Chu, J., Amorin, M. & Ghadiri, M. R. “Asingle-molecule nanopore device detects DNA polymerase activity withsingle-nucleotide resolution.” J. Am. Chem. Soc. 130, 818-820 (2008),the disclosures of which are incorporated herein by reference in theirentireties).

Some embodiments can utilize methods involving the real-time monitoringof DNA polymerase activity. Nucleotide incorporations can be detectedthrough fluorescence resonance energy transfer (FRET) interactionsbetween a fluorophore-bearing polymerase and γ-phosphate-labelednucleotides as described, for example, in U.S. Pat. No. 7,329,492 andU.S. Pat. No. 7,211,414 (each of which is incorporated herein byreference) or nucleotide incorporations can be detected with zero-modewaveguides as described, for example, in U.S. Pat. No. 7,315,019 (whichis incorporated herein by reference) and using fluorescent nucleotideanalogs and engineered polymerases as described, for example, in U.S.Pat. No. 7,405,281 and U.S. Patent Application Publication No.2008/0108082 (each of which is incorporated herein by reference). Theillumination can be restricted to a zeptoliter-scale volume around asurface-tethered polymerase such that incorporation of fluorescentlylabeled nucleotides can be observed with low background (Levene, M. J.et al. “Zero-mode waveguides for single-molecule analysis at highconcentrations.” Science 299, 682-686 (2003); Lundquist, P. M. et al.“Parallel confocal detection of single molecules in real time.” Opt.Lett. 33, 1026-1028 (2008); Korlach, J. et al. “Selective aluminumpassivation for targeted immobilization of single DNA polymerasemolecules in zero-mode waveguide nanostructures.” Proc. Natl. Acad. Sci.USA 105, 1176-1181 (2008), the disclosures of which are incorporatedherein by reference in their entireties).

The above SBS methods can be advantageously carried out in multiplexformats such that multiple different target nucleic acids aremanipulated simultaneously. In particular embodiments, different targetnucleic acids can be treated in a common reaction vessel or on a surfaceof a particular substrate. This allows convenient delivery of sequencingreagents, removal of unreacted reagents and detection of incorporationevents in a multiplex manner. In embodiments using surface-bound targetnucleic acids, the target nucleic acids can be in an array format. In anarray format, the target nucleic acids can be typically bound to asurface in a spatially distinguishable manner. The target nucleic acidscan be bound by direct covalent attachment, attachment to a bead orother particle or binding to a polymerase or other molecule that isattached to the surface. The array can include a single copy of a targetnucleic acid at each site (also referred to as a feature) or multiplecopies having the same sequence can be present at each site or feature.Multiple copies can be produced by amplification methods such as, bridgeamplification or emulsion PCR as described in further detail below.

The methods set forth herein can use arrays having features at any of avariety of densities including, for example, at least about 10features/cm², 100 features/cm², 500 features/cm², 1,000 features/cm²,5,000 features/cm², 10,000 features/cm², 50,000 features/cm², 100,000features/cm², 1,000,000 features/cm², 5,000,000 features/cm², or higher.

It will be appreciated that any of the above-described sequencingprocesses can be incorporated into the methods and/or systems describedherein. For example, the methods or systems can utilize sequencingreagents having mixtures of two or more nucleotide monomers or canotherwise be carried out under conditions where two or more nucleotidemonomers contact a target nucleic acid in a single sequencing cycle.Alternatively or additionally, the methods or systems set forth abovecan be used to obtain a sequence representation at single nucleotideresolution. As set forth in further detail below, a combination ofsequence representations at low resolution and at single nucleotideresolution, can be advantageous for evaluating long sequences, forexample, on a genome wide scale, for extending read length and/or forimproving confidence in sequencing results via error checking.Furthermore, it will be appreciated that other known sequencingprocesses can be easily by implemented for use with the methods and/orsystems described herein.

Removing Nucleotide Monomers and/or Pyrophosphate

Some of the methods described herein include a step of removing asubstance from a site. A site can include a site of nucleotide monomerincorporation and/or a site of detection of monomer incorporation. Asubstance can include, for example, any constituent of a sequencingreagent, any product of incorporating one or more nucleotide monomersinto a polynucleotide complementary to a target nucleic acid, such aspyrophosphate, a target nucleic acid, a polymerase, a cleaved label, apolynucleotide complementary to a target nucleic acid. In a preferredembodiment, one or more nucleotide monomers are removed from a site. Inanother preferred embodiment, pyrophosphate is removed from a site. Ineven more preferred embodiments, both nucleotide monomers andpyrophosphate are removed from a site. Removing a substance can includea variety of methods, for example, washing a substance from a site,diluting a substance from a site, sequestering a substance from a site,degrading a substance, inactivating a substance and denaturing asubstance.

In certain embodiments of the methods described herein, any portion of asubstance can be removed from a site. In particular embodiments,approximately 1%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% and95% of a substance can be removed from a site. In preferred embodiments,approximately 100% of a substance can be removed from a site.

In particular embodiments of the methods described herein, a portion ofa sequencing reagent can be removed from a site of nucleotide monomerincorporation and/or a site of detection of monomer incorporation. Asequencing reagent can be removed from a site subsequent to providingthe sequencing agent to a target nucleic acid in the presence ofpolymerase. In preferred embodiments, a sequencing reagent can beremoved from a site before providing a subsequent sequencing reagent toa target nucleic acid in the presence of polymerase. In any of theabove-described embodiments, the sequencing reagent can be the first,second, third, fourth, fifth or any subsequent sequencing reagent thatis provided.

In some embodiments, an unincorporated nucleotide monomer can be removedfrom a site. In certain embodiments, an unincorporated nucleotidemonomer can be removed from a site of nucleotide monomer incorporationand/or detection after providing the nucleotide monomer to a targetnucleic acid. In more embodiments, an unincorporated nucleotide monomercan be removed from a site before providing a subsequent sequencingreagent to a target nucleic acid.

In some embodiments of the methods described herein, pyrophosphate canbe removed from a site. In certain embodiments, pyrophosphate can beremoved from a site of nucleotide monomer incorporation and/or detectionafter detecting incorporation one or more nucleotide monomers into apolynucleotide. In other embodiments, pyrophosphate can be removed froma site of nucleotide monomer incorporation and/or detection beforeproviding a subsequent sequencing reagent to a target nucleic acid.

In some embodiments, a polynucleotide complementary to a target nucleicacid can be removed from a site. In certain embodiments, apolynucleotide complementary to a target nucleic acid can be removedfrom the target nucleic acid subsequent to performing a first run ofsequencing on the target nucleic acid. In particular embodiments, apolynucleotide complementary to a target nucleic acid can be removedfrom the target nucleic acid before performing a second, third, or anysubsequent run of sequencing on the target nucleic acid.

It will be understood that, in some embodiments, a substance can beremoved from a site at any time before, during or subsequent to a roundof sequencing.

Detection of Incorporated Nucleotide Monomers

Some of the methods described herein include a detection step fordetecting the incorporation of nucleotide monomers into apolynucleotide. Nucleotide monomers may be incorporated into at least aportion of a polynucleotide complementary to the target nucleic acid. Incertain embodiments, at least a portion of the sequencing reagent, whichcomprises unincorporated nucleotide monomers, may be removed from thesite of incorporation/detection prior to detecting incorporatednucleotide monomers.

A variety of methods can be used to detect the incorporation ofnucleotide monomers into a polynucleotide. In preferred methods,pyrophosphate released on incorporation of a nucleotide monomer into apolynucleotide can be detected using pyrosequencing techniques. Asdescribed above, pyrosequencing detects the release of pyrophosphate asparticular nucleotides are incorporated into a nascent polynucleotide(Ronaghi, M., Karamohamed, S., Pettersson, B., Uhlen, M. and Nyren, P.(1996) “Real-time DNA sequencing using detection of pyrophosphaterelease.” Analytical Biochemistry 242(1), 84-9; Ronaghi, M. (2001)“Pyrosequencing sheds light on DNA sequencing.” Genome Res. 11(1), 3-11;Ronaghi, M., Uhlen, M. and Nyren, P. (1998) “A sequencing method basedon real-time pyrophosphate.” Science 281(5375), 363, the disclosures ofwhich are incorporated herein by reference in their entireties).

In some embodiments, at least a portion of the ATP and non-incorporatednucleotides can be removed from the site of incorporation and/ordetection. In preferred embodiments, the ATP and non-incorporatednucleotides can be removed subsequent to a detection step and prior to adelivery. Removing the ATP and non-incorporated nucleotides can include,for example, a washing step, and a degrading step using an enzyme suchas apyrase (Ronaghi M, Karamohamed S, Pettersson B, Uhlen M, Nyren P.“Real-time DNA sequencing using detection of pyrophosphate release.”Analytical Biochemistry. (1996) 242:84-89; Ronaghi M, Uhlen M, Nyren P.“A sequencing method based on real-time pyrophosphate.” Science (1998)281:363, the disclosures of which are hereby incorporated by referencein their entireties).

In some embodiments, at least a portion of released pyrophosphate can beremoved from the site of incorporation and/or detection. In preferredembodiments, the released pyrophosphate can be removed subsequent to adetection step and prior to a delivery. In more embodiments, thereleased pyrophosphate can be removed prior to a delivery.

In more embodiments, incorporation of nucleotide monomers can bedetected using nucleotide monomers comprising labels. Labels can includechromophores, enzymes, antigens, heavy metals, magnetic probes, dyes,phosphorescent groups, radioactive materials, chemiluminescent moieties,scattering or fluorescent nanoparticles, Raman signal generatingmoieties, and electrochemical detecting moieties. Such labels are knownin the art some of which are exemplified previously herein or aredisclosed, for example, in U.S. Pat. No. 7,052,839; Prober, et. al.,Science 238: 336-41 (1997); Connell et. al., BioTechniques 5(4)-342-84(1987); Ansorge, et. al., Nucleic Acids Res. 15(11): 4593-602 (1987);and Smith et. al., Nature 321:674 (1986), the disclosures of which arehereby incorporated by reference in their entireties. In preferredembodiments, a label can be a fluorophore. Exemplary embodiments includeU.S. Pat. No. 7,033,764, U.S. Pat. No. 5,302,509, U.S. Pat. No.7,416,844, and Seo et al. “Four color DNA sequencing by synthesis on achip using photocleavable fluorescent nucleotides,” Proc. Natl. Acad.Sci. USA 102: 5926-5931 (2005), which are herein incorporated byreference in their entireties.

Labels can be attached to the α, β, or γ phosphate, base, or sugarmoiety, of a nucleotide monomer (U.S. Pat. No. 7,361,466; Zhu et al.,“Directly Labelled DNA Probes Using Fluorescent Nucleotides withDifferent Length Linkers,” Nucleic Acids Res. 22: 3418-3422 (1994), andDoublie et al., “Crystal Structure of a Bacteriophage T7 DNA ReplicationComplex at 2.2 Å Resolution,” Nature 391:251-258 (1998), which arehereby incorporated by reference in their entireties). Attachment can bewith or without a cleavable linker between the label and the nucleotide.

In some embodiments, a label can be detected while it is attached to anincorporated nucleotide monomer. In such embodiments, unincorporatedlabeled nucleotide monomers can be removed from the site ofincorporation and/or the site of detection prior to detecting the label.

Alternatively, a label can be detected subsequent to release from anincorporated nucleotide monomer. Release can be through cleavage of acleavable linker, or on incorporation of the nucleotide monomer into apolynucleotide where the label is linked to the β or γ phosphate of thenucleotide monomer, namely, where released pyrophosphate is labeled.

In some embodiments, at least a portion of unincorporated labelednucleotide monomers can be removed from the site of incorporation and/ordetection. In preferred embodiments, at least a portion ofunincorporated labeled nucleotide monomers can be removed prior todetecting the incorporated labeled nucleotide. In more preferredembodiments, approximately 50%, 60%, 70%, 80%, 90%, and 100% ofunincorporated labeled nucleotide monomers can be removed prior todetecting the incorporated labeled nucleotide. In even more preferredembodiments, a label can be removed subsequent to a detection step andprior to a delivery. For example, a fluorescent label linked to anincorporated nucleotide monomer can be removed by cleaving the labelfrom the nucleotide, or photobleaching the dye.

Exemplary embodiments of methods for detecting released labeledpyrophosphate include using nanochannels, using flowcells to separateand detect labeled pyrophosphate from unincorporated nucleotidemonomers, and using mass spectroscopy (U.S. Pat. No. 7,361,466; U.S.Pat. No. 6,869,764; and U.S. Pat. No. 7,052,839, which are herebyincorporated by reference in their entireties). Released pyrophosphatemay also be detected directly, for example, using sensors such asnanotubes (U.S. Patent Application Publication No. 2006/0,199,193, whichis hereby incorporated by reference in its entirety). In preferredembodiments, at least a portion of released pyrophosphate is removedfrom the site of incorporation and/or detection subsequent to thedetection step and prior to a delivery. In more preferred embodiments,approximately 50%, 60%, 70%, 80%, 90%, 100% of released pyrophosphate isremoved from the site of incorporation and/or detection subsequent tothe detection step and prior to a delivery.

In some embodiments described herein, detection of the signal, such aslight emitted form conversion of ATP and luciferin, or light emittedform a fluorescent label, is detected using a charge coupled device(CCD) camera. In other embodiments, a CMOS detector is used. Detectioncan occur on a CMOS array as described, for example, in Agah et al., “AHigh-Resolution Low-Power Oversampling ADC with Extended-Range forBio-Sensor Arrays”, IEEE Symposium 244-245 (2007) and Eltoukhy et al.,“A 0.18 μm CMOS bioluminescence detection lab-on-chip”, IEEE Journal ofSolid-State Circuits 41: 651-662 (2006), the disclosures of which areincorporated herein by reference in their entireties. In addition, itwill be appreciated that other signal detecting devices as known in theart can be used to detect signals produced as a result of nucleotidemonomer incorporation into a polynucleotide complementary to a targetnucleic acid.

Variable Resolution Sequencing of Target Nucleic Acids

Some embodiments described herein include methods for obtaining longsequence reads with high resolution sequence data for a portion of atarget nucleic acid in one or more single sequencing runs (rounds ofsequencing). A portion of a target nucleic acid can include any portionof a target nucleic acid, for example, approximately 1%, 5%, 10%, 20%,30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or, 99%. In certain embodiments,a portion of a target nucleic acid can include a contiguous sequence. Acontiguous portion can be measured as a percentage of a larger fragmentas above or in terms of the number of nucleotides sequenced. Forexample, the portion can be about 10, 20, 30, 40, 50, 100, 150, 200, 250or 500 nucleotides or more. Alternatively, a portion of a target nucleiccan include a plurality of non-contiguous sequences. For example, aportion of a target nucleic acid can include two ends of a targetnucleic acid. Typically the two ends are the same length, but they neednot be and the two ends of a larger fragment that are sequenced at highresolution can differ in length. Again, each end can have a length thatis measured as a percentage of the larger fragment, including forexample, the percentages listed above or as a number of nucleotidesincluding, for example, the numbers listed above.

In certain methods, a sequencing run can comprise more than one seriesof nucleotide monomer delivery steps in which the number of nucleotidemonomers can vary. For example, a sequencing run can include a series ofsingle nucleotide monomer delivery steps to yield high resolutionsequence information, and also include a series of multiple nucleotidemonomer delivery steps to yield low resolution sequence information. Itwill be understood that a sequencing run can include any combination ofnucleotide monomer delivery step, for example, single, doublet, ortriplet delivery steps. In many embodiments, conditions can be used thatresult in longer extension lengths for the cycles that are carried outwith a series of multiple nucleotide monomer delivery steps compared tothe extension lengths resulting from single nucleotide monomer deliverysteps.

In an exemplary embodiment, a sequencing run can include a series ofconsecutive single nucleotide delivery steps where dATP, dCTP, dGTP, anddTTP are each provided to a target nucleic acid in subsequent deliverysteps. Such delivery steps can yield sequence information at highresolution. The sequencing run can also include a series of consecutivedoublet delivery steps where, for example, dATP/dCTP are supplied in asingle delivery step, and dGTP/dTTP are supplied in a subsequentdelivery steps. Such delivery steps can yield long lengths of sequenceinformation, albeit at a lower resolution.

Several cycles can be carried out using single nucleotide deliverysteps, followed by several cycles where a sequencing reagent havingseveral different nucleotide types is delivered, and then followed byseveral cycles of single nucleotide delivery steps. Such methods can beused as a means to provide sequence of a target nucleic acid, whereinthe sequence obtained at each end of the target nucleic acid is of highresolution and the sequence obtained from the middle portion is at alower resolution. Although the exact nucleotide sequence of the middle,low resolution portion is not known, the number of nucleotide monomerincorporation events in this portion can be determined. As such, theapproximate length of the combined sequenced portion of the targetnucleic acid (both high resolution and lower resolution sequenceportions) can be determined. The sequence of the middle portion need notbe determined at single nucleotide resolution. Furthermore, the highresolution end portion sequences of the target nucleic acid can be usedto enhance assembly, for example, of long homopolymer regions. Methodsfor assembling a long sequence, such as a genome, from paired-endsequences of several fragments thereof are known in the art and can beapplied to the methods set forth herein. Exemplary methods are describedin WO 2007/010252, WO 2008/041002, U.S. Patent Application PublicationNo. 2006/0024681, and U.S. Patent Application Publication No.2006/0292611, each of which is incorporated herein by reference. In thisway, high sequence resolution methodology can be employed whendetermining accurate nucleotide sequence is important and low resolutionmethodology can be employed when extending the sequence read length isvaluable but knowledge of the sequence of the target nucleic acid regionthat is sequenced is not important.

High Resolution Sequence Acquisition Via Multiple Rounds of LowResolution Sequencing

Nucleic acid sequence information can be obtained from two or morerounds of low resolution sequencing carried out on the same targetnucleic acid. A first low resolution sequence representation can beobtained for a target nucleic acid, using methods set forth herein. Thefirst low resolution sequence representation can be degenerate withrespect to two or more nucleotide types. As exemplified in the upperchart of FIG. 2, a first predicted sequence obtained from cycles ofsequencing using mixtures of A/C and G/T is degenerate with respect totwo pairs of nucleotide types, G/T and A/C. Following the first round oflow resolution sequencing, the products of the first round can beremoved leaving the target nucleic acid in condition for a second roundof sequencing. A second low resolution sequence representation for thetarget nucleic acid can be obtained using similar methods except that atleast one of the two or more nucleotide types in the first lowresolution sequence representation is different from at least one of thetwo or more nucleotide types in the second low resolution sequencerepresentation. Looking again to FIG. 2, the middle chart is exemplaryof a second predicted sequence obtained from cycles of sequencing usingmixtures of A/G and C/T, resulting in a low resolution sequence that isdegenerate with respect to C/T and A/G. The two low resolution sequencescan be compared to determine the actual sequence of the target nucleicacid at single nucleotide resolution as shown in the lower chart of FIG.2. Mixtures of nucleotide monomers can be used additionally oralternatively to those exemplified above including, for example, variousdoublet mixtures or triplet mixtures such as those set forth elsewhereherein.

The above methods can be carried out for a plurality of target nucleicacids, for example, in a multiplex format. In such embodiments, multiplelow resolution sequence representations can be associated withindividual target nucleic acid molecules and used to determine theactual sequence of the target nucleic acid at single nucleotideresolution. Taking an array format as an example, a plurality of firstlow resolution sequence representations can be obtained after a firstround of sequencing, each of the low resolution sequence representationsbeing associated with known features on the array. Following the firstround of low resolution sequencing the array can be treated, for exampleusing denaturing conditions to remove extension products of the firstround of sequencing and to return the single stranded target nucleicacids at each feature to a state that is ready for a second round ofsequencing. Then a plurality of second low resolution sequencerepresentations can be obtained from a second round of sequencing, eachof the low resolution sequence representations being associated withknown features on the array. By comparing the two low resolutionsequence representations at each feature, the actual sequence of thetarget nucleic acid at each feature can be determined at singlenucleotide resolution.

In particular embodiments, low resolution sequence representations canbe obtained for a plurality of target nucleic acids that are fragmentsof a larger nucleic acid such as a genome. In such embodiments, thesequence information for the individual fragments can be used todetermine the actual sequence of the larger nucleic acid at singlenucleotide resolution. For example, multiple low resolution sequencerepresentations from each feature can be used to determine the actualsequence of each fragment target nucleic acid at single nucleotideresolution. The actual sequence of each fragment can then be used todetermine the actual sequence of the larger sequence, for example, byalignment to a reference sequence or by de novo assembly methods. In analternative embodiment, the low resolution sequence representations fromdifferent features can be used directly to determine the actual sequenceof the larger sequence, for example, using pattern matching methods.

Low resolution sequence representations can provide a signature fordifferent nucleic acids in a sample. Accordingly, the actual sequence ofa target nucleic acid need not be determined at single-nucleotideresolution and, instead, a low resolution sequence representation of thenucleic acid can be used. In particular embodiments, a low resolutionsequence representation can be used to determine the presence or absenceof a target nucleic acid in a particular sample or to quantify theamount of the target nucleic acid. Exemplary applications include, butare not limited to, expression analysis, identification of organisms, orevaluation of structure for chromosomes, expressed RNAs or other nucleicacids as set forth in further detail below.

In particular embodiments, low resolution sequence representations forone or more target mRNA molecules can be used to determine expressionlevels in one or more samples of interest. So long as the low resolutionsequence representations are sufficiently indicative of the mRNA, theactual sequence need not be known at single nucleotide resolution. Forexample, if a low resolution sequence representation distinguishes atarget mRNA from all other mRNA species expressed in a target sample andin a reference sample, then comparison of the low resolution sequencerepresentations from both samples can be used to determine relativeexpression levels. Target nucleic acids used in expression methods canbe obtained from any of a variety of different samples including, forexample, cells, tissues or biological fluids from organisms such asthose set forth above. Presence or absence, or even quantities of targetnucleic acids can be determined for samples that have been treated withdifferent chemical agents, physical manipulations, environmentalconditions or the like. Alternatively or additionally, samples can befrom organisms that are experiencing any of a variety of diseases,conditions, developmental states or the like. Typically, a referencesample and target sample will differ in regard to one or more of theabove factors (for example, treatment, conditions, species origin, orcell type).

In particular embodiments, low resolution sequence representations fortarget nucleic acids obtained from a particular organism can be used tocharacterize or identify the organism. For example, a pathogenicorganism can be identified in an environmental sample or in a clinicalsample from an individual based on at least one low resolution sequencerepresentation for a target nucleic acid from the sample. So long as theone or more low resolution sequence representations are sufficientlyindicative of the organism, the actual sequence need not be known atsingle nucleotide resolution. For example, if a low resolution sequencerepresentation distinguishes a pathogenic bacterial strain from otherbacteria, then comparison of the low resolution sequence representationsfrom the sample of interest to low resolution sequence representationsfrom reference samples or from a database can be used to detect presenceor absence of the pathogenic bacterial strain.

In further embodiments, the structure of a chromosome, RNA or othernucleic acid can be determined based on low resolution sequencerepresentations. For example, if a low resolution sequencerepresentation distinguishes a chromosomal region from other regions ofa chromosome, then comparison of the low resolution sequencerepresentations from a target sample and a reference sample for whichthe chromosome structure is known can be used to identify insertions,deletions or rearrangements in the target sample. Similarly, if a lowresolution sequence representation distinguishes a target mRNA isoform(i.e. alternative splice product of a gene) from another mRNA isoformexpression product of the same gene, then comparison of the lowresolution sequence representations for both isoforms can be used todetermine presence or absence of the target isoform. Target nucleicacids used to determine chromosome or RNA structure can be obtained fromany of a variety of samples including, but not limited to thoseexemplified above.

In some embodiments, one or more steps are carried out by a computer.For example, low resolution sequence representations can be provided toa computer that is programmed to compare representations to each other,determine an actual sequence of a target nucleic acid at singlenucleotide resolution, identify samples from which a low resolutionsequence representation was derived or the like. Exemplary computersystems that are useful in the invention include, but are not limited topersonal computer systems, such as those based on Intel®, IBM®, orMotorola® microprocessors; or work stations such as a SPARC workstationor UNIX workstation. Useful systems include those using the MicrosoftWindows, UNIX or LINUX operating system. The systems and methodsdescribed herein can also be implemented to run on client-server systemsor wide-area networks such as the Internet.

A computer system useful in the invention can be configured to operateas either a client or server and can include one or more processorswhich are coupled to a random access memory (RAM). Implementation ofembodiments of the present invention is not limited to any particularenvironment or device configuration. The embodiments of the presentinvention may be implemented in any type of computer system orprocessing environment capable of supporting the methodologies which areset forth herein. In particular embodiments, algorithms can be writtenin MATLAB, C or C++, or other computer languages known in the art.

The computer can be further programmed to store one or more of therepresentations and the actual sequence. The computer can be programmedto transmit one or more of the representations, the actual sequence orother relevant information to a user, another computer, a database or anetwork. The computer can also be programmed to receive relevantinformation from a user, another computer, a database or a network. Suchinformation can include data, such as signals or images, obtained from asequencing method, one or more reference sequences, characteristics ofan organism of interest or the like.

Preparation of Amplified Target Nucleic Acids

In some embodiments, a target nucleic acid can be amplified for use withthe methods described herein. Such embodiments include preparingamplified libraries of target nucleic acids. Library preparation can beaccomplished by random fragmentation of DNA, followed by in vitroligation of common adaptor sequences.

Various protocols can be used to generate an array of millions ofspatially immobilized PCR colonies, sometimes referred to as polonies,on a substrate. For example, such clonally clustered amplicons of targetnucleic acids can be generated by in situ polonies, emulsion PCR, orbridge PCR (Mitra, R. D. & Church, G. M. “In situ localizedamplification and contact replication of many individual DNA molecules.”Nucleic Acids Res. 27, e34 (1999); Dressman, D., Yan, H., Traverso, G.,Kinzler, K. W. & Vogelstein, B. “Transforming single DNA molecules intofluorescent magnetic particles for detection and enumeration of geneticvariations.” Proc. Natl. Acad. Sci. USA 100, 8817-8822 (2003); Adessi,C. et al. “Solid phase DNA amplification: characterisation of primerattachment and amplification mechanisms.” Nucleic Acids Res. 28, e87(2000); Fedurco, M., Romieu, A., Williams, S., Lawrence, I. & Turcatti,G. “BTA, a novel reagent for DNA attachment on glass and efficientgeneration of solid-phase amplified DNA colonies.” Nucleic Acids Res.34, e22 (2006), each of which is incorporated by reference herein intheir entireties).

In embodiments using emulsion PCR, an in vitro-constructed adaptorflanked shotgun library can be PCR amplified in a water-in-oil emulsion.The PCR is multi-template PCR, because only a single primer pair isused. One of the PCR primers is tethered to the surface (5′-attached) ofmicron-scale beads that are also included in the reaction. A lowtemplate concentration results in most bead-containing compartmentshaving either zero or one template molecule present. In productiveemulsion compartments (where both a bead and template molecule ispresent), PCR amplicons can be captured to the surface of the bead.After breaking the emulsion, beads bearing amplification products can beselectively enriched. Each clonally amplified bead will bear on itssurface PCR products corresponding to amplification of a single moleculefrom the template library. Various embodiments of emulsion PCR methodsthat are useful are set forth in U.S. Patent Application Publication No.2005/0042648; U.S. Patent Application Publication No. 2005/0079510; U.S.Patent Application Publication No. 2005/0130173 and WO 05/010145, eachof which is incorporated herein by reference.

In embodiments using bridge PCR, also known as cluster PCR, an invitro-constructed adaptor-flanked shotgun library can be PCR amplifiedusing primers coated densely on the surface of a substrate. The primersare attached at their 5′ ends by a flexible linker. Amplificationproducts originating from any given member of the template libraryremain locally tethered near the point of origin. At the conclusion ofthe PCR, each clonal cluster contains ˜1,000 copies of a single memberof the template library. Accurate measurement of the concentration ofthe template library can be used to optimize the cluster density whilesimultaneously avoiding overcrowding. Various embodiments of bridge PCRmethods that are useful are set forth in U.S. Patent ApplicationPublication No. 2007/0128624, WO 07/010,251, U.S. Pat. No. 6,090,592 andU.S. Pat. No. 5,641,658, each of which is incorporated herein byreference.

Such embodiments, can generate PCR amplicons derived from any givensingle library molecule that are spatially separated, for example, atdiscrete sites or features on a planar substrate (in situ polonies,bridge PCR), or to the surface of micron-scale beads, which can berecovered and arrayed (emulsion PCR).

Clusters in Wells

More techniques that can used with the methods described herein includethe preparation of substrates with target nucleic acids and/or enzymesattached to the surface of substrate. In some embodiments, the substratecomprises one or more wells. Such embodiments are especiallyadvantageous, in pyroseqeuncing where the shape and depth of the wellscan be optimized for fluidic delivery of reagents between detectionsteps, and for reducing diffusion of pyrophosphate during detectionsteps.

In an exemplary embodiment, modified primers and enzymes can be attachedto the surface of wells by coating the wells with a linking compound,for example activated dextran. The dextran can be activated by includinggroups that are reactive to amines, for example, aldehyde. The surfaceof the wells can be reacted with amino modified primers, for example, aprimer P1 and a primer P2. Such primers can be used for bridge PCR atthe surface of the well. In addition, the surface of the wells can bereacted with peptides having a biotin moiety. The biotin moiety can beused to an intermediary coupling agent, for example, a streptavidinagent. Biotinylated enzymes can be attached to the surface of the wellthrough the intermediary coupling agent. Wells having target nucleicacids and/or enzymes attached thereto, can be used with the methodsdescribed herein. As will be appreciated, the amount of primers andenzymes on the well surface can be optimized by various methods,including for example, by optimizing the density of reactants on thesurface of the wells.

Cluster Formation by Re-Seeding

Additional techniques that can be used with the methods described hereininclude processes for increasing the number of wells or other featureson a substrate that contain clusters. In many SBS applications,substrate features or wells may not be efficiently used because many ofthe features or wells lack a target nucleic acid. The process describedbelow, which is termed reseeding, can include the steps of (1) seedingthe substrate with a target nucleic acid, (2) performing limited cyclesof bridge amplification on the target nucleic acid, and (3) re-seedingthe substrate with the target nucleic acid and repeating theamplification step. In some embodiments, several cycles of re-seedingcan be used to further increase the number of wells containing targetnucleic acids.

In an exemplary embodiment, a substrate comprises a plurality of wellswherein the wells further comprise attached primers, namely, primer P1and primer P2. P1 and P2 can hybridize to adapter sequences present on asample comprising a plurality of different target nucleic acids. In afirst seeding, the target nucleic acids can be seeded to the substratein a diffuse concentration such that each well may be seeded with asingle target nucleic acid only. Accordingly, many of the wells may notbe occupied with a target nucleic acid.

Bridge amplification can be carried out for a limited number of cycles,for example, 5-15 cycles. Each well with a target nucleic acid is likelyto contain a plurality of amplified target nucleic acid, for example,30-50 target nucleic acid molecules.

In a second seeding, the substrate can be re-seeded with the samplecomprising a plurality of different target nucleic acids, in a diffuseconcentration such that each well may be seeded from the sample with asingle target nucleic acid only. More wells will now be seeded with asingle target nucleic acid, however, some of the wells that werepreviously seeded and amplified may contain more than one type targetnucleic acid.

Bridge amplification can be repeated for a limited number of cycles, forexample, 5-15 cycles. Under these conditions, more wells will have beennewly seeded with target single target nucleic acids and will yield auniform population of template copies.

Wells that were seeded in the first and second seedings may contain alarge amount of the first seeded target nucleic acid, and a much loweramount of the second seeded target nucleic acid. The seeding step andbridge amplification step can be repeated, for example, one or moretimes, so that it is likely that a well will contain a single targetnucleic acid or a small amount of an additional target nucleic acid.

The conditions for number of cycles for seeding the wells and bridgeamplification, and the number of cycles for bridge amplification can beoptimized such the additional target nucleic acid in a well containingmore than one type of target nucleic acid is unlikely to be amplified toa level that adversely affects the signal-to-noise ratio in sequencingreactions.

Some embodiments of the above-described processes can be applied tosubstrates that do not comprise wells. For example, substrates having asurface with a contiguous reactive surface capable of attaching toseveral spatially separated molecules of interest (or colonies ofmolecules of interest). An exemplary substrate is a Solexa flow cell.However, the re-seeding methods provide particular advantageous inembodiments using substrates with a patterned surface of features, forexample, a surface which may comprise one or more reactive pads orwells. Substrates having features that are spatially separated in arepeated or otherwise ordered pattern may be desired over largecontiguous surfaces to which different molecules are randomly depositedto form features. For example, a relatively high density of features canbe provided in the case of the former while reducing the probability, onone hand, of overlapping features which can occur in the case of thelatter when the surface is too densely populated, and, on the otherhand, the probability of unused space in the case of the latter when thesurface is too diffusely populated. Also, the presence of a non-randompattern can make detection more efficient in some embodiments by easingresource requirements for accurate image registration and precisepinpointing of information content on the surface. Re-seeding can allowa larger fraction of the features on a patterned surface to be occupiedcompared to other methods of depositing molecules of interest only once.

EXAMPLES Example 1 Single, Doublet and Triplet Delivery Methods SingleDelivery Method

Using a pyrosequencing methodology, in a first flow step, a sequencingreagent comprising dATP is provided to a target nucleic acid in thepresence of polymerase. If dATP is incorporated into the polynucleotidecomplementary to the target nucleic acid, a signal proportional to thenumber of incorporated units of nucleotide monomers is produced anddetected. Subsequent to this flow step unincorporated dATP is washedaway.

In a second flow step, a sequencing reagent comprising dCTP is providedto a target nucleic acid in the presence of polymerase. If dCTP isincorporated into the polynucleotide complementary to the target nucleicacid, a signal proportional to the number of incorporated units ofnucleotide monomers is produced and detected. Subsequent to this flowstep unincorporated dCTP is washed away.

In a third flow step, a sequencing reagent comprising dGTP is providedto a target nucleic acid in the presence of polymerase. If dGTP isincorporated into the polynucleotide complementary to the target nucleicacid, a signal proportional to the number of incorporated units ofnucleotide monomers is produced and detected. Subsequent to this flowstep unincorporated dGTP is washed away.

In a fourth flow step, a sequencing reagent comprising dTTP is providedto a target nucleic acid in the presence of polymerase. If dTTP isincorporated into the polynucleotide complementary to the target nucleicacid, a signal proportional to the number of incorporated units ofnucleotide monomers is produced and detected. Subsequent to this flowstep unincorporated dTTP is washed away.

The first, second, third and fourth flow, detection and wash steps arerepeated for a total of 500 deliveries. For the round of sequencing,sequence information of the target nucleic acid is obtained. A readlength of less than 300 base pairs is obtained (FIG. 1).

Doublet Delivery Method

Using a pyrosequencing methodology, in a first flow step, a sequencingreagent comprising dATP and dCTP is provided to a target nucleic acid inthe presence of polymerase. If dATP and/or dCTP are incorporated intothe polynucleotide complementary to the target nucleic acid, a signalproportional to the number of incorporated units of nucleotide monomersis produced and detected. Subsequent to this flow step unincorporateddATP and dCTP are washed away.

In a second flow step, a sequencing reagent comprising dGTP and dTTP isprovided to the target nucleic acid. If dGTP and/or dTTP areincorporated into the polynucleotide complementary to the target nucleicacid, a signal proportional to the number of incorporated units ofnucleotide monomers is produced and detected. Subsequent to this flowstep unincorporated dGTP and dTTP are washed away.

The first and second flow, detection, and wash steps are repeated for atotal of 500 deliveries. For the round of sequencing, sequenceinformation of the target nucleic acid is obtained. A read length ofapproximately 900 base pairs is obtained (FIG. 1).

Triplet Delivery Method

Using a pyrosequencing methodology, in a first flow step, a sequencingreagent comprising dATP, dCTP, and dGTP is provided to a target nucleicacid in the presence of polymerase. If dATP, dCTP, and/or dGTP areincorporated into the polynucleotide complementary to the target nucleicacid, a signal proportional to the number of incorporated units ofnucleotide monomers is produced and detected. Subsequent to this flowstep unincorporated dATP, dCTP, and/or dGTP are washed away.

In a second flow step, a sequencing reagent comprising dTTP is providedto a target nucleic acid in the presence of polymerase. If dTTP isincorporated into the polynucleotide complementary to the target nucleicacid, a signal proportional to the number of incorporated units ofnucleotide monomers is produced and detected. Subsequent to this flowstep unincorporated dTTP is washed away.

The first and second flow, detection and wash steps are repeated for atotal of 500 deliveries. For the round of sequencing, sequenceinformation of the target nucleic acid is obtained. A read length ofapproximately 1650 base pairs is obtained (FIG. 1).

In some alternative embodiments, nucleotide monomers used in a previousflow step are incorporated in subsequent flow steps. In otherembodiments, it is possible to change the composition of the firstand/or second sequencing reagent before the end of the sequencing run.The following example provides an illustration of each of thesealternatives applied to a single sequencing round.

In a first flow step, a sequencing reagent comprising dATP, dCTP, anddGTP is provided to a target nucleic acid in the presence of polymerase.If dATP, dCTP, and/or dGTP are incorporated into the polynucleotidecomplementary to the target nucleic acid, a signal proportional to thenumber of incorporated units of nucleotide monomers is produced anddetected. Subsequent to this flow step unincorporated dATP, dCTP, and/ordGTP are washed away.

In a second flow step, a sequencing reagent comprising dATP, dCTP, anddTTP is provided to a target nucleic acid in the presence of polymerase.If dATP, dCTP, and/or dTTP are incorporated into the polynucleotidecomplementary to the target nucleic acid, a signal proportional to thenumber of incorporated units of nucleotide monomers is produced anddetected. Subsequent to this flow step unincorporated dATP, dCTP, and/ordTTP are washed away.

In a third flow step, a sequencing reagent comprising dATP, dGTP, anddTTP is provided to a target nucleic acid in the presence of polymerase.If dATP, dGTP, and/or dTTP are incorporated into the polynucleotidecomplementary to the target nucleic acid, a signal proportional to thenumber of incorporated units of nucleotide monomers is produced anddetected. Subsequent to this flow step unincorporated dATP, dGTP, and/ordTTP are washed away.

In a fourth flow step, a sequencing reagent comprising dCTP, dGTP, anddTTP is provided to a target nucleic acid in the presence of polymerase.If dCTP, dGTP, and/or dGTP are incorporated into the polynucleotidecomplementary to the target nucleic acid, a signal proportional to thenumber of incorporated units of nucleotide monomers is produced anddetected. Subsequent to this flow step unincorporated dCTP, dGTP, and/ordTTP are washed away.

The first, second, third and fourth flow, detection and wash steps arerepeated for a total of 500 deliveries. For the round of sequencing,sequence information of the target nucleic acid is obtained. A readlength of approximately 1650 base pairs is obtained (FIG. 1).

Example 2 High Resolution Sequencing of a Target Nucleic Acid

This example demonstrates a method of obtaining high resolution sequenceinformation using a doublet delivery process. This example isillustrated in FIG. 2. To begin, a first round of sequencing isperformed on a target nucleic acid using a doublet delivery methodaccording to Example 1 and as shown in the upper chart of FIG. 2. Thefirst flow step includes providing a first sequencing reagent comprisingdATP and dCTP to the target nucleic acid. A 1× signal intensity isdetected in the first cycle, indicative of a single nucleotide monomerincorporation. The second flow step includes providing a secondsequencing reagent comprising dGTP and dTTP to the target nucleic acid.A 2× signal intensity is detected in the second cycle, indicative of twonucleotide monomer incorporations. The first and second flow, detection,and wash steps are repeated for a total of 8 cycles. For the first roundof sequencing, a 1^(st) predicted sequence of the target nucleic acid isobtained. Accordingly a low resolution sequence representation coveringa read length of 12 base pairs is obtained.

In the next round of the high resolution sequencing process, thepolynucleotide complementary to the target nucleic acid is removed. Asecond round of sequencing is then performed on the target nucleic acidusing a doublet delivery method according to Example 1 except thestarting doublet combination is changed as shown in the middle chart ofFIG. 2. For example, in the second round, the first flow step includesproviding a first sequencing reagent comprising dATP and dGTP to thetarget nucleic acid. A 3× signal intensity is detected in the firstcycle, indicative of three nucleotide monomer incorporations. The secondflow step includes providing a second sequencing reagent comprising dCTPand dTTP to the target nucleic acid. A 2× signal intensity is detectedin the second cycle, indicative of two nucleotide monomerincorporations. The first and second flow, detection, and wash steps arerepeated for a total of 6 cycles. For the second round of sequencing, a2^(nd) predicted sequence of the target nucleic acid is obtained.Accordingly low resolution sequence representation covering a readlength of 12 base pairs is obtained.

Sequence information from the first and second rounds of sequencing iscombined and a high resolution sequence of the target nucleic acid isobtained as shown in the lower chart of FIG. 2.

Example 3 High/Low Resolution Sequencing of Target Nucleic Acids

In some applications, for example, in paired end sequencing, it can beadvantageous to obtain long lengths of sequence information at a lowerresolution, while obtaining sequence information for the flanking endsof the target nucleic acid at a higher resolution. In some applications,a combination of delivery methods can be applied in a round ofsequencing.

In a round of sequencing, a single delivery method and a tripletdelivery method are applied to obtain high resolution sequenceinformation for 100 bp of each end of a 1500 bp target nucleic acid. Asingle delivery method is applied to obtain sequencing information forthe first 100 bp of the target nucleic acid, then a triplet deliverymethod is applied to obtain sequence information for the next 1300 bp ofthe target nucleic acid, then a single delivery method is applied toobtain sequence information for final 100 base pairs of the 1500 bptarget nucleic acid.

The above description discloses several methods and systems of thepresent invention. This invention is susceptible to modifications in themethods and materials, as well as alterations in the fabrication methodsand equipment. Such modifications will become apparent to those skilledin the art from a consideration of this disclosure or practice of theinvention disclosed herein. For example, the invention has beenexemplified using nucleic acids but can be applied to other polymers aswell. Consequently, it is not intended that this invention be limited tothe specific embodiments disclosed herein, but that it cover allmodifications and alternatives coming within the true scope and spiritof the invention.

All references cited herein including, but not limited to, published andunpublished applications, patents, and literature references, areincorporated herein by reference in their entirety and are hereby made apart of this specification. To the extent publications and patents orpatent applications incorporated by reference contradict the disclosurecontained in the specification, the specification is intended tosupersede and/or take precedence over any such contradictory material.

The term “comprising” as used herein is synonymous with “including,”“containing,” or “characterized by,” and is inclusive or open-ended anddoes not exclude additional, unrecited elements or method steps.

1-19. (canceled)
 20. A method of making an array of nucleic acidcolonies, comprising (a) providing a substrate comprising a patternedsurface of features, wherein the features are spatially organized in arepeating pattern on the surface of the substrate; (b) contacting thesubstrate with a solution of different target nucleic acids to seed nomore than a subset of the features that contact the solution; (c)amplifying the nucleic acids on the subset of features; and (d)repeating steps (b) and (c) to increase the number of features that areseeded with a nucleic acid, thereby making an array of nucleic acidcolonies.
 21. The method of claim 20, further comprising detecting thearray of nucleic acid colonies in a sequencing reaction.
 22. The methodof claim 21, wherein a subset of the colonies in the array comprise afirst type of target nucleic acid and a second type of target nucleicacid.
 23. The method of claim 22, wherein the amount of the second typeof target nucleic acid does not adversely affect the signal-to-noise forthe detecting of the first type of nucleic acid.
 24. The method of claim21, wherein the detecting comprises detecting a byproduct ofincorporating a nucleotide into a nucleic acid.
 25. The method of claim24, wherein the byproduct is pyrophosphate.
 26. The method of claim 21,wherein the sequencing reaction comprises extension of a nascent nucleicacid strand through iterative addition of nucleotides against templatesin the nucleic acid colonies.
 27. The method of claim 26, wherein thenucleotides comprise fluorescent labels that are detected in thesequencing reaction.
 28. The method of claim 20, wherein the featurescomprise wells.
 29. The method of claim 20, wherein the featurescomprise attached primer nucleic acids for the amplifying.
 30. Themethod of claim 29, wherein each of the features comprises a pair ofattached primer nucleic acids.
 31. The method of claim 30, wherein theamplifying comprises bridge amplification.
 32. The method of claim 29,wherein the amplifying comprises polymerase chain reactionamplification.
 33. The method of claim 29, wherein the nucleic acidcolonies are covalently attached to the features.
 34. The method ofclaim 20, wherein the features comprise reactive pads on the surface.35. The method of claim 20, wherein the features are spatially separatedfrom each other on the surface of the substrate.
 36. The method of claim20, wherein the same solution of different target nucleic acids iscontacted with the substrate in steps (b) and (d).
 37. The method ofclaim 20, wherein the substrate comprises a CMOS detector.
 38. Themethod of claim 20, wherein the substrate comprises a density of atleast 1,000 features/cm².
 39. The method of claim 20, wherein eachfeature in the subset is seeded with no more than a single nucleic acidfrom the solution during step (b).